← FDA Drug Approvals (Drugs@FDA)
PATADAY ONCE DAILY RELIEF
NDA · New Drug Application · Sponsor: ALCON LABS INC · Approved 2004-12-22
Drug application
- FDA Application #
NDA021545- Application type
- New Drug Application
- Brand name
- PATADAY ONCE DAILY RELIEF
- Generic name
- OLOPATADINE HYDROCHLORIDE
- Active ingredients
- OLOPATADINE HYDROCHLORIDE
- Dosage form
- SOLUTION/DROPS
- Route
- OPHTHALMIC
- Marketing status
- Over-the-counter
- Sponsor
- ALCON LABS INC
- Manufacturer
- Alcon Laboratories, Inc.
- First approval
- 2004-12-22
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown