Nafcillin
- Product NDC
- 67850-031
- 11-digit product format
- 678500031
- Labeler code
- 67850
- Product ID
- 67850-031_b6678852-7186-4357-afd8-03fd07fb8b6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin Injection
- Dosage form
- POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Methapharm Inc.
- Application
- ANDA090560
- Marketing category
- ANDA
- Marketing start
- 2019-03-05
- Marketing end
- 0000-00-00
- Substance
- NAFCILLIN SODIUM
- Active strength
- 1 g/g
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67850-031 | NAFCILLIN (NAFCILLIN INJECTION) POWDER, FOR SOLUTION [METHAPHARM INC.] | 8 | Legacy NDC | 20241207_4376871a-91c7-4730-b58d-62a2b6915de5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67850-031-10 | 67850003110 | 10 VIAL in 1 CARTON (67850-031-10) > 1 g in 1 VIAL | 10 vial | 2019-03-05 | 0000-00-00 | No | No | Current |