Metronidazole
- Product NDC
- 68001-229
- 11-digit product format
- 680010229
- Labeler code
- 68001
- Product ID
- 68001-229_990934e3-cd98-993f-e053-2a95a90a766e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA070035
- Marketing category
- ANDA
- Marketing start
- 2014-03-13
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68001-229-00 | 68001022900 | 100 TABLET in 1 BOTTLE, PLASTIC (68001-229-00) | 100 tablet | 2014-03-13 | 0000-00-00 | No | No | Current |
| 68001-229-13 | 68001022913 | 250 TABLET in 1 BOTTLE, PLASTIC (68001-229-13) | 250 tablet | 2014-03-13 | 0000-00-00 | No | No | Current |