Minocycline hydrochloride
- Product NDC
- 50090-1838
- 11-digit product format
- 500901838
- Labeler code
- 50090
- Product ID
- 50090-1838_6ac40934-9c2b-4852-bb57-e18423ac2bc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2000-12-22
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 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