metronidazole
- Product NDC
- 70934-915
- 11-digit product format
- 709340915
- Labeler code
- 70934
- Product ID
- 70934-915_d5e2af82-ee85-58a7-e053-2a95a90a2316
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA206560
- Marketing category
- ANDA
- Marketing start
- 2021-10-21
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-915-14 | 70934091514 | 14 TABLET in 1 BOTTLE, PLASTIC (70934-915-14) | 14 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 70934-915-20 | 70934091520 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-915-20) | 20 tablet | 2022-01-10 | 0000-00-00 | No | No | Current |
| 70934-915-21 | 70934091521 | 21 TABLET in 1 BOTTLE, PLASTIC (70934-915-21) | 21 tablet | 2021-10-25 | 0000-00-00 | No | No | Current |
| 70934-915-30 | 70934091530 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-915-30) | 30 tablet | 2021-11-15 | 0000-00-00 | No | No | Current |