NAFCILLIN SODIUM
- Product NDC
- 83270-310
- 11-digit product format
- 832700310
- Labeler code
- 83270
- Product ID
- 83270-310_4c94ba3a-3e85-06b7-e063-6394a90a7034
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NAFCILLIN SODIUM
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Application
- ANDA200002
- Marketing category
- ANDA
- Marketing start
- 2026-02-20
- Substance
- NAFCILLIN SODIUM
- Active strength
- 2 g/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
- NAFCILLIN SODIUM
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAFCILLIN SODIUM | 2 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 49G3001BCK |
| Rxcui | 1721458, 1721460 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83270-310-10 | NAFCILLIN SODIUM | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 2 |
| 83270-310-10 | NAFCILLIN SODIUM | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 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 |
|---|
| 83270-310-10 | 83270031010 | 10 VIAL in 1 CARTON (83270-310-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2026-02-20 | No | No | Historical |