Tinidazole
- Product NDC
- 63629-8386
- 11-digit product format
- 636298386
- Labeler code
- 63629
- Product ID
- 63629-8386_e90ddd19-e65d-42a8-9bb5-1dad0383b2bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tinidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202044
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- Marketing end
- 0000-00-00
- Substance
- TINIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-8386-1 | 63629838601 | 4 TABLET in 1 BOTTLE (63629-8386-1) | 4 tablet | 2020-11-10 | 0000-00-00 | No | No | Current |