Quick answers
- What is Bicillin C-R 900/300?
- Bicillin C-R 900/300 is a brand name of Penicillin g benzathine and penicillin g procaine, a prescription medicine. The FDA NDC Directory lists 1 Bicillin C-R 900/300 product in 1 strength and form.
- Who makes Bicillin C-R 900/300?
- King Pharms LLC holds the FDA application for Bicillin C-R 900/300 (NDA050138, approved May 18, 1953).
- Is there a generic or store brand of Bicillin C-R 900/300?
- Other products of Penicillin g benzathine and penicillin g procaine are listed with the FDA, but none in exactly the same strength and form as a Bicillin C-R 900/300 product.
- Has Bicillin C-R 900/300 been recalled?
- No recall linked to Bicillin C-R 900/300 products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Bicillin C-R 900/300 is
Each Bicillin C-R 900/300 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 benzathine and penicillin g procaine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| penicillin g benzathine 900000 units/2 mL · penicillin g procaine 300000 units/2 mL injection, suspension (intramuscular) | Bicillin C-R 900/300 | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Penicillin g benzathine and penicillin g procaine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA050138 | King Pharms LLC | May 18, 1953 | 1 |
Companies that list Bicillin C-R 900/300
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Bicillin C-R 900/300 products.
- Pfizer Laboratories Div Pfizer Inc1 product
Recalls
No recall linked to Bicillin C-R 900/300 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.