Ampicillin
- Product NDC
- 67457-351
- 11-digit product format
- 674570351
- Labeler code
- 67457
- Product ID
- 67457-351_d5f1a48b-28c5-4264-b2ca-d21f7d105578
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA201025
- Marketing category
- ANDA
- Marketing start
- 2016-09-12
- Marketing end
- 2024-05-31
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-351-10 | 67457035110 | 10 VIAL in 1 CARTON (67457-351-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (67457-351-01) | 10 vial | 2016-09-12 | 0000-00-00 | No | No | Current |