Metronidazole
- Product NDC
- 69043-005
- 11-digit product format
- 690430005
- Labeler code
- 69043
- Product ID
- 69043-005_b8baa39f-cc67-4e5d-b061-cbba132342a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cronus Pharma LLC
- Application
- ANDA203974
- Marketing category
- ANDA
- Marketing start
- 2015-05-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69043-005-01 | 69043000501 | 100 TABLET in 1 BOTTLE (69043-005-01) | 100 tablet | 2015-05-29 | 0000-00-00 | No | No | Current |
| 69043-005-05 | 69043000505 | 500 TABLET in 1 BOTTLE (69043-005-05) | 500 tablet | 2015-05-29 | 0000-00-00 | No | No | Current |