Nafcillin
- Product NDC
- 0781-3125
- 11-digit product format
- 007813125
- Labeler code
- 0781
- Product ID
- 0781-3125_ad046eb4-32af-4468-9b2e-88accc706d03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA062527
- Marketing category
- ANDA
- Marketing start
- 1984-08-02
- Marketing end
- 0000-00-00
- Substance
- NAFCILLIN SODIUM
- Active strength
- 2 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3125-95 | 00781312595 | 10 VIAL in 1 PACKAGE (0781-3125-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3125-85) | 10 vial | 1984-08-08 | 0000-00-00 | No | No | Current |