← FDA Drug Approvals (Drugs@FDA)
MINOCYCLINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS LTD · Approved 2019-12-03
Drug application
- FDA Application #
ANDA091118- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- MINOCYCLINE HYDROCHLORIDE
- Generic name
- Minocycline Hydrochloride
- Active ingredients
- MINOCYCLINE HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- SUN PHARM INDS LTD
- First approval
- 2019-12-03
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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