Minocycline
- Product NDC
- 63629-2228
- 11-digit product format
- 636292228
- Labeler code
- 63629
- Product ID
- 63629-2228_770d045f-00fb-48ac-9faa-616f5c054d43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065131
- Marketing category
- ANDA
- Marketing start
- 2003-04-16
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [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 |
|---|
| 63629-2228-1 | 63629222801 | 50 TABLET in 1 BOTTLE (63629-2228-1) | 50 tablet | 2021-03-22 | 0000-00-00 | No | No | Current |