Minocycline hydrochloride
- Product NDC
- 33261-871
- 11-digit product format
- 332610871
- Labeler code
- 33261
- Product ID
- 33261-871_b467b2f6-9ecd-45be-a714-664764233d01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2000-12-22
- 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
- 2019-12-31
- 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 |