AMPICILLIN
- Product NDC
- 51662-1595
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPICILLIN
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA062719
- Marketing category
- ANDA
- Substance
- AMPICILLIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 51662-1595-3 | 10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 2022-08-18 | | No | Historical |