Minocycline Hydrochloride
- Product NDC
- 71335-2564
- 11-digit product format
- 713352564
- Labeler code
- 71335
- Product ID
- 71335-2564_52dee53a-6622-45b3-a222-880f3c47a50c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065470
- Marketing category
- ANDA
- Marketing start
- 2008-03-11
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 71335-2564-1 | 71335256401 | 30 CAPSULE in 1 BOTTLE (71335-2564-1) | 30 capsule | 2025-01-28 | No | No | Historical |
| 71335-2564-2 | 71335256402 | 60 CAPSULE in 1 BOTTLE (71335-2564-2) | 60 capsule | 2025-01-28 | No | No | Historical |
| 71335-2564-3 | 71335256403 | 16 CAPSULE in 1 BOTTLE (71335-2564-3) | 16 capsule | 2025-01-28 | No | No | Historical |