Minocycline Hydrochloride
- Product NDC
- 72162-2574
- 11-digit product format
- 721622574
- Labeler code
- 72162
- Product ID
- 72162-2574_47237f2b-fe4f-4786-9009-7de16a602ec1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2015-04-02
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72162-2574-2 | 72162257402 | 50 CAPSULE in 1 BOTTLE (72162-2574-2) | 50 capsule | 2025-11-17 | No | No | Historical |
| 72162-2574-5 | 72162257405 | 500 CAPSULE in 1 BOTTLE (72162-2574-5) | 500 capsule | 2025-11-17 | No | No | Historical |