Metronidazole
- Product NDC
- 50090-0214
- 11-digit product format
- 500900214
- Labeler code
- 50090
- Product ID
- 50090-0214_dd4ac59e-9b91-4d24-b9b2-ef224925766a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203458
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0214-0 | 50090021400 | 4 TABLET, FILM COATED in 1 BOTTLE (50090-0214-0) | 2014-11-28 | 0000-00-00 | No | No | Current |