Metronidazole
- Product NDC
- 0904-1453
- 11-digit product format
- 009041453
- Labeler code
- 0904
- Product ID
- 0904-1453_cf44bf25-c2e0-4350-ae6b-9d92659f0aff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA070027
- Marketing category
- ANDA
- Marketing start
- 1998-08-08
- Marketing end
- 2023-05-31
- Substance
- METRONIDAZOLE
- Active strength
- 250 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 |
|---|
| 0904-1453-61 | 00904145361 | 100 BLISTER PACK in 1 CARTON (0904-1453-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 1998-08-08 | 0000-00-00 | No | No | Current |