AMPICILLIN
- Product NDC
- 71872-7204
- 11-digit product format
- 718727204
- Labeler code
- 71872
- Product ID
- 71872-7204_fae21111-25f7-bf9a-e053-6294a90ab215
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin Injection
- Dosage form
- POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2019-03-06
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/g
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JFN36L5S8K | AMPICILLIN SODIUM | 69-52-3 | AMPICILLIN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7204-1 | 71872720401 | 1 VIAL in 1 BAG (71872-7204-1) / 1 g in 1 VIAL | 1 vial | 2020-02-13 | No | No | Historical |