Ampicillin
- Product NDC
- 71872-7169
- 11-digit product format
- 718727169
- Labeler code
- 71872
- Product ID
- 71872-7169_8a0e1d98-b474-1b29-e053-2995a90a82ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2018-08-01
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 2 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7169-1 | 71872716901 | 1 VIAL in 1 BAG (71872-7169-1) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2019-05-23 | 0000-00-00 | No | No | Current |