FDA
Olopatadine Hydrochloride
The FDA lists this product in 33 strengths and forms.
Composition
- Active ingredients
- OLOPATADINE HYDROCHLORIDE EQ 0.2% BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · Solution/dropsANDA203152-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · Solution/dropsANDA206046-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE · Solution/dropsANDA209015-001 · Tentative approval
- OLOPATADINE HYDROCHLORIDE 0.665MG/SPRAY · Spray, meteredANDA213757-001 · Discontinued
- OLOPATADINE HYDROCHLORIDE EQ 0.2% BASE · Solution/dropsANDA217051-001 · Discontinued
- OLOPATADINE HYDROCHLORIDE EQ 0.2% BASE · Solution/dropsANDA090918-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · Solution/dropsANDA204392-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.2% BASE · Solution/dropsANDA209752-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · Solution/dropsANDA078350-001 · Over the counter
- OLOPATADINE HYDROCHLORIDE EQ 0.2% BASE · Solution/drops
At a glance
- Brand name
- Olopatadine Hydrochloride
- Route
- Eye
- Dosage form
- Solution/drops
- Applicant
- Sciegen Pharms
- Status
- Discontinued
- FDA approval
- 5 Dec 2017
- Application
- ANDA204723-001