Metronidazole
- Product NDC
- 60687-424
- 11-digit product format
- 606870424
- Labeler code
- 60687
- Product ID
- 60687-424_c183bfe7-8bc1-1096-e053-2a95a90ad512
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA070772
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- Marketing end
- 2021-05-31
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60687-424-01 | 60687042401 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-424-01) > 1 TABLET in 1 BLISTER PACK (60687-424-11) | 100 blister pack | 2019-05-13 | 0000-00-00 | No | No | Current |