Nafcillin
- Product NDC
- 0781-3126
- 11-digit product format
- 007813126
- Labeler code
- 0781
- Product ID
- 0781-3126_9484b358-fb99-40e5-a31f-fdd68dac517a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA062527
- Marketing category
- ANDA
- Marketing start
- 2017-08-01
- Marketing end
- 0000-00-00
- Substance
- NAFCILLIN SODIUM
- Active strength
- 10 g/100mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3126-95 | 00781312695 | 10 BOTTLE in 1 CARTON (0781-3126-95) > 100 mL in 1 BOTTLE (0781-3126-46) | 10 bottle | 2017-08-01 | 0000-00-00 | No | No | Current |