metronidazole
- Product NDC
- 68071-2449
- 11-digit product format
- 680712449
- Labeler code
- 68071
- Product ID
- 68071-2449_c4c2c757-4ee2-643f-e053-2a95a90a1e17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA206560
- Marketing category
- ANDA
- Marketing start
- 2019-02-23
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-2449 | METRONIDAZOLE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210616_c4c2c757-4ee1-643f-e053-2a95a90a1e17.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2449-4 | 68071244904 | 4 TABLET in 1 BOTTLE (68071-2449-4) | 4 tablet | 2021-06-15 | 0000-00-00 | No | No | Current |