Details for New Drug Application (NDA): 204620
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The generic ingredient in OLOPATADINE HYDROCHLORIDE is olopatadine hydrochloride. There are seventeen drug master file entries for this compound. Forty-six suppliers are listed for this compound. Additional details are available on the olopatadine hydrochloride profile page.
Summary for 204620
| Tradename: | OLOPATADINE HYDROCHLORIDE |
| Applicant: | Rising |
| Ingredient: | olopatadine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 204620
| Mechanism of Action | Histamine H1 Receptor Antagonists |
| Physiological Effect | Decreased Histamine Release |
Medical Subject Heading (MeSH) Categories for 204620
Suppliers and Packaging for NDA: 204620
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| OLOPATADINE HYDROCHLORIDE | olopatadine hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 204620 | ANDA | Rising Pharma Holdings, Inc. | 16571-861 | 16571-861-25 | 1 CONTAINER in 1 CARTON (16571-861-25) / 2.5 mL in 1 CONTAINER |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | EQ 0.2% BASE | ||||
| Approval Date: | Jun 16, 2020 | TE: | RLD: | No | |||||
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