Bicillin CR is a brand name of Penicillin g benzathine and penicillin g procaine, a prescription medicine. The FDA NDC Directory lists 2 Bicillin CR products in 1 strength and form.

Who makes Bicillin CR?

King Pharms LLC holds the FDA application for Bicillin CR (NDA050138, approved May 18, 1953).

Is there a generic or store brand of Bicillin CR?

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 CR product.

Bicillin CR (Penicillin g benzathine and penicillin g procaine): maker, FDA approval and generic versions

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Bicillin CR?: Bicillin CR is a brand name of Penicillin g benzathine and penicillin g procaine, a prescription medicine. The FDA NDC Directory lists 2 Bicillin CR products in 1 strength and form.
Who makes Bicillin CR?: King Pharms LLC holds the FDA application for Bicillin CR (NDA050138, approved May 18, 1953).
Is there a generic or store brand of Bicillin CR?: 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 CR product.
Has Bicillin CR been recalled?: No recall linked to Bicillin CR products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Bicillin CR is

Each Bicillin CR 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 600000 units/2 mL · penicillin g procaine 600000 units/2 mL injection, suspension (intramuscular)	Bicillin CR	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.

FDA applications of Bicillin CR products (Drugs@FDA)
Application	Holder	First approved	Products
NDA050138	King Pharms LLC	May 18, 1953	2

Companies that list Bicillin CR

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Bicillin CR products.

Pfizer Laboratories Div Pfizer Inc2 products

Recalls

No recall linked to Bicillin CR 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.

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Bicillin CR