metronidazole
- Product NDC
- 71335-2681
- 11-digit product format
- 713352681
- Labeler code
- 71335
- Product ID
- 71335-2681_3215cc0e-fb94-4009-aeb5-7ccaf36dfcbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206560
- Marketing category
- ANDA
- Marketing start
- 2019-02-23
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- metronidazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METRONIDAZOLE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 140QMO216E |
| Rxcui | 311681 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2681-1 | 71335268101 | 14 TABLET in 1 BOTTLE (71335-2681-1) | 14 tablet | 2025-09-12 | No | No | Historical |
| 71335-2681-2 | 71335268102 | 3 TABLET in 1 BOTTLE (71335-2681-2) | 3 tablet | 2025-09-12 | No | No | Historical |
| 71335-2681-3 | 71335268103 | 9 TABLET in 1 BOTTLE (71335-2681-3) | 9 tablet | 2025-09-12 | No | No | Historical |
| 71335-2681-4 | 71335268104 | 10 TABLET in 1 BOTTLE (71335-2681-4) | 10 tablet | 2025-09-12 | No | No | Historical |