NDC 60793-702
Bicillin L-A 2400000 [iU] per 4 mL injection, suspension
On the label: Pfizer Laboratories Div Pfizer Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| King Pharmaceuticals LLC | Rochester, MI, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 18, 2025 · 11 inspections, 2 with FDA action |
Recalls
- Jul 10, 2025 · Class II · Pfizer Inc.
CGMP Deviations; particulates identified during visual inspection
Lots: Lots: HJ3235, Exp 09/30/26; GL2954, HP6222, Exp, 01/31/27; HR9967, Exp 05/31/27; HP6232, LT5190,Exp 09/30/27; HP6228, Exp 10/31/27; - Jul 10, 2025 · Class II · Pfizer Inc.
CGMP Deviations; particulates identified during visual inspection
Lots: Lots GT2598, GT2599, Exp 09/30/26; HK2909, Exp 02/28/27; HR9969, Exp 04/30/27; HR9984, Exp 08/31/27.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Penicillin G: every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 2400000 [iU] per 4 mL
- Approval
- NDA NDA050141
- On the market since
- Jun 27, 1952
- Package NDCs
60793-702-0460793-702-10- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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