Nafcillin
- Product NDC
- 83270-316
- 11-digit product format
- 832700316
- Labeler code
- 83270
- Product ID
- 83270-316_5d271b3d-8ac1-de0d-e063-6394a90a99f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Application
- ANDA203830
- Marketing category
- ANDA
- Marketing start
- 2026-10-12
- Substance
- NAFCILLIN SODIUM
- Active strength
- 10 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Source provenance: Browse the complete Orange Book source catalog.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nafcillin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAFCILLIN SODIUM | 10 g/1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 83270-316-10 | 83270031610 | 10 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (83270-316-10) | 2026-10-12 | No | No | Current |