Metronidazole
- Product NDC
- 68001-263
- 11-digit product format
- 680010263
- Labeler code
- 68001
- Product ID
- 68001-263_c7017f81-b071-51c9-e053-2995a90a43b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA070044
- Marketing category
- ANDA
- Marketing start
- 2014-09-24
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-263-03 | 68001026303 | 500 TABLET in 1 BOTTLE, PLASTIC (68001-263-03) | 500 tablet | 2014-09-24 | 0000-00-00 | No | No | Current |