← FDA Drug Approvals (Drugs@FDA)
MINOCYCLINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS INC · Approved 2013-05-13
Drug application
- FDA Application #
ANDA090867
- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- MINOCYCLINE HYDROCHLORIDE
- Generic name
- MINOCYCLINE HYDROCHLORIDE
- Active ingredients
- MINOCYCLINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- SUN PHARM INDS INC
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- First approval
- 2013-05-13
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown