Metronidazole
- Product NDC
- 70934-813
- 11-digit product format
- 709340813
- Labeler code
- 70934
- Product ID
- 70934-813_b8df4b69-4e36-6f79-e053-2995a90ad33e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA203974
- Marketing category
- ANDA
- Marketing start
- 2021-01-13
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-813-21 | 70934081321 | 21 TABLET in 1 BOTTLE, PLASTIC (70934-813-21) | 21 tablet | 2021-01-13 | 0000-00-00 | No | No | Current |