Metronidazole
- Product NDC
- 70518-0090
- 11-digit product format
- 705180090
- Labeler code
- 70518
- Product ID
- 70518-0090_f2027140-58fe-5c24-e053-2a95a90adfe5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070027
- Marketing category
- ANDA
- Marketing start
- 2016-12-28
- 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
- 2024-12-31
- 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 |
|---|
| 70518-0090-0 | 70518009000 | 28 TABLET in 1 BOTTLE (70518-0090-0) | 28 tablet | 2016-12-28 | 0000-00-00 | No | No | Current |