Metronidazole
- Product NDC
- 43063-021
- 11-digit product format
- 430630021
- Labeler code
- 43063
- Product ID
- 43063-021_db709af3-fdeb-400d-e053-2995a90aa9c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA070033
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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 |
|---|
| 43063-021-04 | 43063002104 | 4 TABLET in 1 BOTTLE, PLASTIC (43063-021-04) | 4 tablet | 2010-09-01 | 0000-00-00 | No | No | Current |