Nafcillin
- Product NDC
- 0409-3714
- 11-digit product format
- 004093714
- Labeler code
- 0409
- Product ID
- 0409-3714_9ed6b8d3-5000-40d6-880f-58f256099af3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, 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 |
|---|
| 0409-3714-01 | 00409371401 | 10 VIAL in 1 PACKAGE (0409-3714-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-3714-10) | 10 vial | 2017-08-01 | 0000-00-00 | No | No | Current |