Ampicillin
- Product NDC
- 66794-222
- 11-digit product format
- 667940222
- Labeler code
- 66794
- Product ID
- 66794-222_f091d2b5-3f8e-1060-e053-2995a90a1697
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Piramal Critical Care Inc
- Application
- ANDA090583
- Marketing category
- ANDA
- Marketing start
- 2020-03-09
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66794-222-41 | 66794022241 | 10 VIAL in 1 CARTON (66794-222-41) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (66794-222-02) | 10 vial | 2020-03-09 | 0000-00-00 | No | No | Current |