Ampicillin
- Product NDC
- 83270-312
- 11-digit product format
- 832700312
- Labeler code
- 83270
- Product ID
- 83270-312_519efe7d-db24-3b5e-e063-6394a90a427d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Application
- ANDA201025
- Marketing category
- ANDA
- Marketing start
- 2026-02-27
- Substance
- AMPICILLIN SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ampicillin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMPICILLIN SODIUM | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JFN36L5S8K |
| Rxcui | 1721473, 1721474, 1721475, 1721476 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83270-312-10 | Ampicillin | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 1 |
| 83270-312-10 | Ampicillin | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83270-312-10 | 83270031210 | 10 VIAL in 1 CARTON (83270-312-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2026-02-27 | No | No | Historical |