Nafcillin
- Product NDC
- 25021-198
- 11-digit product format
- 250210198
- Labeler code
- 25021
- Product ID
- 25021-198_f50e7f65-8bca-4df1-bff1-8069b33def90
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA090005
- Marketing category
- ANDA
- Marketing start
- 2025-04-15
- Substance
- NAFCILLIN SODIUM
- Active strength
- 10 g/100mL
- 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
- Nafcillin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAFCILLIN SODIUM | 10 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 49G3001BCK |
| Rxcui | 239189 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 25021-198-99 | Nafcillin | 100 mL in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 100 | | 1 |
| 25021-198-99 | Nafcillin | 1 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-198 | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 1 | Current NDC, 2 package rows | 20250504_a6a4e122-b7f5-4eb5-8555-7aea6eda794b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 25021-198-99 | 25021019899 | 1 VIAL in 1 CARTON (25021-198-99) / 100 mL in 1 VIAL | 1 vial | 2025-04-15 | No | No | Current |