Quick answers
- What is Pfizerpen?
- Pfizerpen is a brand name of Penicillin g, a prescription medicine. The FDA NDC Directory lists 4 Pfizerpen products in 2 strengths and forms.
- Who makes Pfizerpen?
- Pfizer holds the FDA application for Pfizerpen (ANDA060657, approved August 30, 1968).
- Is there a generic or store brand of Pfizerpen?
- Other products of Penicillin g are listed with the FDA, but none in exactly the same strength and form as a Pfizerpen product.
- Has Pfizerpen been recalled?
- No recall linked to Pfizerpen products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Pfizerpen is
Each Pfizerpen product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Penicillin g · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| penicillin g potassium 20000000 units powder, for solution (intravenous) | Pfizerpen | None listed | DailyMed |
| penicillin g potassium 5000000 units powder, for solution (intramuscular, intrapleural, intrathecal, intravenous) | Pfizerpen | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Penicillin g →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA060657 | Pfizer | August 30, 1968 | 4 |
Companies that list Pfizerpen
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Pfizerpen products.
- Roerig4 products
Recalls
No recall linked to Pfizerpen products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.