Nafcillin Sodium
- Product NDC
- 0781-3129
- 11-digit product format
- 007813129
- Labeler code
- 0781
- Product ID
- 0781-3129_d6d562a8-3aa3-424b-8849-15c607bc172e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA062732
- Marketing category
- ANDA
- Marketing start
- 1986-12-23
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3129-92 | 00781312992 | 10 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0781-3129-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0781-3129-15) | 2005-09-23 | 0000-00-00 | No | No | Current |