Metronidazole
- Product NDC
- 70518-0324
- 11-digit product format
- 705180324
- Labeler code
- 70518
- Product ID
- 70518-0324_e76330bc-cc64-fa16-e053-2995a90a7ab9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070027
- Marketing category
- ANDA
- Marketing start
- 2017-03-16
- 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
- 2023-12-31
- 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 |
|---|
| 70518-0324-0 | 70518032400 | 28 TABLET in 1 BOTTLE, PLASTIC (70518-0324-0) | 28 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |
| 70518-0324-1 | 70518032401 | 30 TABLET in 1 BLISTER PACK (70518-0324-1) | 30 tablet | 2021-08-21 | 0000-00-00 | No | No | Current |
| 70518-0324-2 | 70518032402 | 21 TABLET in 1 BOTTLE, PLASTIC (70518-0324-2) | 21 tablet | 2021-10-06 | 0000-00-00 | No | No | Current |