Minocycline Hydrochloride
- Product NDC
- 68071-2311
- 11-digit product format
- 680712311
- Labeler code
- 68071
- Product ID
- 68071-2311_d5904f6c-5b27-1465-e053-2995a90a427e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065470
- Marketing category
- ANDA
- Marketing start
- 2008-03-11
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 50 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
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 |
|---|
| 68071-2311-3 | 68071231103 | 30 CAPSULE in 1 BOTTLE (68071-2311-3) | 30 capsule | 2020-12-10 | 0000-00-00 | No | No | Current |