Minocycline Hydrochloride
- Product NDC
- 70518-0055
- 11-digit product format
- 705180055
- Labeler code
- 70518
- Product ID
- 70518-0055_80124b30-256c-2276-e053-2991aa0ab315
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA063181
- Marketing category
- ANDA
- Marketing start
- 2016-12-12
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record