← FDA Drug Approvals (Drugs@FDA)
OLOPATADINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: FDC LTD · Approved 2019-09-26
Drug application
- FDA Application #
ANDA209282- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- OLOPATADINE HYDROCHLORIDE
- Generic name
- Olopatadine Hydrochloride
- Active ingredients
- OLOPATADINE HYDROCHLORIDE
- Dosage form
- SOLUTION/DROPS
- Route
- OPHTHALMIC
- Marketing status
- Discontinued
- Sponsor
- FDC LTD
- First approval
- 2019-09-26
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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