Ampicillin
- Product NDC
- 71872-7240
- 11-digit product format
- 718727240
- Labeler code
- 71872
- Product ID
- 71872-7240_fb3345ac-1c37-35c8-e053-6294a90abc4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA062772
- Marketing category
- ANDA
- Marketing start
- 2012-05-10
- Substance
- AMPICILLIN SODIUM
- Active strength
- 2 g/1
- 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 |
| 7C782967RD | AMPICILLIN | 69-53-4 | Ampicillin |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7240-1 | 71872724001 | 1 VIAL in 1 BAG (71872-7240-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2021-02-15 | No | No | Historical |