Pet Drug Reports

Penicillin G Procaine (Norocillin, Go-dry): adverse event reports that FDA received

Active ingredient

Also sold as: Norocillin, Go-dry, MASTI-CLEAR, Pen-G Max, Crysticillin 300 A.S., Formula A-34, and 4 more brand names.

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.

Read this first. FDA says this about the data:

An API dataset query result cannot be used to estimate the risk associated with the product or compare one drug or device product with another. When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event. This dataset should not be the sole source of information for clinical decision-making or other assumptions about the safety or effectiveness of a product. The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine publishes these words. Source: Adverse Event Reports for Animal Drugs and Devices, read on . The data have the reports that FDA received through .

This page is not veterinary advice. For an animal that is ill, speak to a veterinarian.

Contacting a veterinarianHow to report to FDA

From January 1987 to October 2025, FDA received 729 adverse event reports that name a drug with penicillin g procaine as its active ingredient. Of the 729 reports, 202 (27.7%) are about cattle. 99 reports are about horses (13.6%).

In January to March 2026, FDA received no reports that name this drug. The signs that appear in the largest number of the 729 reports are "Death", "Suspension, Abnormal" and "Anaphylaxis". A report is not proof that a drug caused a sign.

Fewer than 20 reports named this drug in the 12 months before June 2026, so this page gives no change. Reports about dogs are 12.8% of the reports that name this drug, and 72.6% of all reports.

Search engines list a drug page with 500 reports or more in all years. The page also needs 30 reports or more in the 12 months to June 2026. This page is under one of these numbers. The site keeps the page and keeps it out of search engines.

Since the last update of the FDA data

The latest update of the FDA data, recorded on , changed no count of this page.

January to March 2026 is the latest closed quarter in the data. In that quarter FDA received 0 reports that name penicillin g procaine: 0 dog, 0 cat, 0 horse, 0 other or not given.

All updatesFeed of updates (RSS)

Signs that the reports list

A sign is a coded term from the report. The words in brackets are a plain gloss of the term. The percentage is the share of the 729 reports that list the sign. One report can list more than one sign.

The sign that is in the largest number of the reports comes first.

  1. Death22.6%165 reports
  2. Suspension, Abnormal[a product quality report, not a sign in an animal]18.9%138 reports
  3. Anaphylaxis[sudden severe allergic-type reaction]11.8%86 reports
  4. Residues in milk9.1%66 reports
  5. Collapse6.2%45 reports
  6. Vomiting3.7%27 reports
  7. Injection site swelling[swelling where the injection was given]3.6%26 reports
  8. Hyperactivity3.3%24 reports
  9. Dyspnoea[difficulty breathing]3.2%23 reports
  10. Injection site abscess[abscess where the injection was given]3%22 reports
  11. Ataxia[unsteady, uncoordinated movement]2.6%19 reports
  12. Shaking2.5%18 reports
  13. Respiratory distress2.3%17 reports
  14. Anorexia[not eating]2.2%16 reports
Show the next 16 signs
  1. Injection site pain[pain where the injection was given]2.2%16 reports
  2. Mammary gland oedema2.1%15 reports
  3. Urticaria[hives]2.1%15 reports
  4. Convulsion[seizure]1.8%13 reports
  5. Fever1.8%13 reports
  6. Product Defect, General[a product quality report, not a sign in an animal]1.8%13 reports
  7. Diarrhoea[diarrhea]1.6%12 reports
  8. Abortion1.5%11 reports
  9. No sign[no clinical sign was reported]1.5%11 reports
  10. Recumbency[lying down and unable or unwilling to rise]1.5%11 reports
  11. Restlessness1.5%11 reports
  12. Confusion1.4%10 reports
  13. Depression[dull, quiet or withdrawn]1.4%10 reports
  14. Hypersalivation[drooling]1.4%10 reports
  15. Underfilling, Package[a product quality report, not a sign in an animal]1.4%10 reports
  16. Containers, Damaged[a product quality report, not a sign in an animal]1.2%9 reports

The list shows 30 of 316 coded signs. A report is not proof that a drug caused a sign. Download all signs (CSV)

Reports by species

The share is of all 729 reports that name penicillin g procaine. The other reports give a different species or no species.

Reports for each month, Jul 2021 to Jun 2026

Dog4 reports

No chart: no month has 5 or more reports.

Cat0 reports

No chart: no month has 5 or more reports.

Horse0 reports

No chart: no month has 5 or more reports.

Other or not given35 reports

No chart: no month has 5 or more reports.

The month is the month in which FDA received the report. Each chart has its own scale. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

Reports by year

  • Dog
  • Cat
  • Horse
  • Other or not given
Reports that name penicillin g procaine, by the year in which FDA received them and by species
YearDogCatHorseOther or not givenAll species
202500088
20241001011
202300099
202230058
202100077
202010045
2019200911
2018310812
20174101015
20167011523
201530047
2014512816
20131221318
2012502815
20113141826
20104102833
20091014446
20081062431
20071121115
20063053442
20054021622
200430121732
200350101025
200210056
20012061422
20004441123
19994052130
199830103447
19971123236
19961101214
19951041217
1994203712
199320237
199220259
1991003811
19902011114
1989600511
1988104712
19871141521

2025 has the reports that FDA received through Oct 2025. Download the years (CSV)

What the reports record

Outcome at the time of the report

  • Recovered/Normal4.9%36
  • Recovered with Sequela[recovered, with a lasting effect]0.4%3
  • Ongoing0.8%6
  • Died24%175
  • Euthanized0.1%1
  • Outcome Unknown2.2%16

An outcome in a report is not proof that the drug caused it. The person who sends the report gives the outcome. Each share is of the 729 reports that name penicillin g procaine.

A report about more than one animal can have more than one outcome.

Kind of report

  • Safety issue66.1%482
  • Lack of expected effectiveness0.1%1
  • Both safety and lack of expected effectiveness0%0
  • Manufacturing or product defect33.3%243
  • Other0.4%3

65 reports say if the event was serious. 66.2% of them have the serious flag. The person who sends the report sets the flag.

Show age, weight, breed and route

Age of the animal

  • Under 1 year11.5%84
  • 1 to 3 years10.7%78
  • 4 to 7 years8.2%60
  • 8 to 11 years4.1%30
  • 12 years and over2.9%21
  • Age not given62.6%456

Weight of the animal

  • Under 5 kg (11 lb)3.3%24
  • 5 to 9.9 kg (11 to 22 lb)4%29
  • 10 to 24.9 kg (22 to 55 lb)1.6%12
  • 25 to 44.9 kg (55 to 99 lb)4.8%35
  • 45 kg and over (99 lb and over)30.5%222
  • Weight not given55.8%407

Breed, where the report gives one breed

A breed with many animals has many reports.

Route in the report

  • Intramuscular30.5%222
  • Intramammary11.5%84
  • Subcutaneous9.3%68
  • Intravenous0.7%5
  • Oral0.5%4
  • Other0.5%4

Each bar is on a scale of 0 to 100%.

Approved animal drugs with this active ingredient (FDA Green Book)

This section is reference data. It has no report count.

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.

Brand names

  • Norocillin
  • Go-dry
  • MASTI-CLEAR
  • Pen-G Max
  • Crysticillin 300 A.S.
  • Formula A-34
  • Uni-Biotic 4 Dose
  • Herdsman’s Choice
  • Dry-A-Cillin
  • Pro-Pen-G

What the Green Book records give

Applications with an approval in force
7
Approved species
Cattle, Sheep, Swine, Cats, Dogs, Equids, Horses
Dose forms
Suspension, Injectable Suspension, Liquid (Suspension)
Routes
Intramammary, Intramuscular
Sale
RX (prescription)
Earliest approval date in the records

The species, dose forms and routes are the words of the Green Book records for all the applications together. One product can have fewer. The label of a product gives its approved use.

Applications in the Green Book of 2 Nov 2026, pioneer applications (NADA) first
Brand nameActive ingredientsSponsorApproved speciesApplication
NorocillinPenicillin G ProcaineNorbrook Laboratories, Ltd.Horses, Cattle, Swine, SheepNADA 065-010
Go-dry; MASTI-CLEARPenicillin G ProcaineHQ Specialty Pharma Corp.CattleNADA 065-081
Pen-G MaxPenicillin G ProcaineHuvepharma EOODDogs, Cats, Horses, Cattle, Swine, SheepNADA 065-110
Crystalline Pro Penicillin GPenicillin G ProcaineZoetis Inc.Dogs, Cats, HorsesNADA 065-130
Crysticillin 300 A.S.Penicillin G ProcaineZoetis Inc.Dogs, Cats, Horses, Cattle, Swine, SheepNADA 065-174
Formula A-34; Uni-Biotic 4 Dose; Herdsman’s Choice; Dry-A-CillinPenicillin G ProcaineBimeda Animal Health Ltd.CattleNADA 065-383
Pro-Pen-GPenicillin G ProcaineBimeda Animal Health Ltd.Horses, Cattle, Swine, SheepNADA 065-505
Penicillin 100 Type A Medicated Article; Penicillin G Procaine 50 Type A Medicated Articleapproval withdrawnPenicillin G ProcaineZoetis Inc.Swine, Chickens, TurkeysNADA 046-666
Penicillin G Procaine 50% Type A Medicated Articleapproval withdrawnPenicillin G ProcainePhibro Animal Health Corp.Swine, Chickens, TurkeysNADA 046-668
Aqua-Mast; Hanfords Four-Penapproval withdrawnPenicillin G ProcaineG.C. Hanford Mfg. Co.CattleNADA 065-465
True Antibiotic Formula #10approval withdrawnPenicillin G ProcaineBoehringer Ingelheim Animal Health USA Inc.Not in the list of major speciesNADA 065-466
Jetpen; Penicillin G Procaine Aqueous Suspensionapproval withdrawnPenicillin G ProcaineNorbrook Laboratories, Ltd.Horses, Cattle, Swine, SheepNADA 065-493

Other pages with this ingredient

A report names a drug by its set of active ingredients. Each set has its own page. The list is in order of name.

Next in the A to Z list

All drugs by active ingredient. Brand names A to Z

FDA pages for this drug

The site checked these addresses on . The links open in a new tab.

Cite this page

Pet Drug Reports. Penicillin G Procaine: adverse event reports that FDA received. https://petdrugreports.com/drug/penicillin-g-procaine/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .

Where the data come from

The counts come from the openFDA Animal and Veterinary adverse event files, export of 30 Oct 2026. The files have the reports that the FDA Center for Veterinary Medicine received through 26 Jun 2026. The files mask brand and manufacturer names. The site counts a drug by the active ingredients that each record gives, and gives no count to a brand, an application or a company. Ingredient names and the lists of approved products follow the FDA Green Book of 2 Nov 2026. The site does not use the application number that a record has.

The site does not publish report text, lot numbers or details of a reporter. FDA's record is the authority. See how the site counts reports, the data sources and the corrections page.

Questions about these reports

Which brand are these reports about?

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand. The Green Book section of this page lists the brand names with this active ingredient.

Do the reports show that the drug caused the signs?

No. FDA states this about the data.

When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event.

The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices

How many reports did FDA receive in the latest 12 months?

FDA received 1 report in the 12 months to June 2026. It received 13 reports in the 12 months before. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

What kinds of report are in the count?

Of the 729 reports received from January 1987 to October 2025, 66.1% are about a safety issue only. 0.1% are about a lack of expected effectiveness, alone or with a safety issue. 33.3% are about a defect of the product or its package.