Minocycline hydrochloride
- Product NDC
- 67296-1144
- 11-digit product format
- 672961144
- Labeler code
- 67296
- Product ID
- 67296-1144_9c9ef8d5-1787-a96d-e053-2995a90a1c70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2000-12-22
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0020414E5U | MINOCYCLINE HYDROCHLORIDE | 13614-98-7 | MINOCYCLINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1144-1 | 67296114401 | 14 CAPSULE in 1 BOTTLE (67296-1144-1) | 14 capsule | 2000-12-22 | 0000-00-00 | No | No | Current |