Ampicillin sodium
- Product NDC
- 72572-093
- 11-digit product format
- 725720093
- Labeler code
- 72572
- Product ID
- 72572-093_4131081c-b618-0dba-e063-6294a90af249
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA201025
- Marketing category
- ANDA
- Marketing start
- 2025-09-08
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ampicillin sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMPICILLIN SODIUM | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JFN36L5S8K |
| Rxcui | 1721475, 1721476 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72572-093-10 | Ampicillin sodium | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 2 |
| 72572-093-10 | Ampicillin sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72572-093-10 | 72572009310 | 10 VIAL in 1 CARTON (72572-093-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2025-09-08 | No | No | Historical |