Details for New Drug Application (NDA): 206276
✉ Email this page to a colleague
The generic ingredient in PATADAY ONCE DAILY RELIEF is olopatadine hydrochloride. There are seventeen drug master file entries for this compound. Forty suppliers are listed for this compound. Additional details are available on the olopatadine hydrochloride profile page.
Summary for 206276
Tradename: | PATADAY ONCE DAILY RELIEF |
Applicant: | Alcon Labs Inc |
Ingredient: | olopatadine hydrochloride |
Patents: | 2 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 206276
Mechanism of Action | Histamine H1 Receptor Antagonists |
Physiological Effect | Decreased Histamine Release |
Medical Subject Heading (MeSH) Categories for 206276
Suppliers and Packaging for NDA: 206276
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PATADAY ONCE DAILY RELIEF | olopatadine hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 206276 | NDA | Alcon Laboratories, Inc. | 0065-0816 | 0065-0816-01 | 2 BOTTLE, PLASTIC in 1 CARTON (0065-0816-01) / 2.5 mL in 1 BOTTLE, PLASTIC |
PATADAY ONCE DAILY RELIEF | olopatadine hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 206276 | NDA | Alcon Laboratories, Inc. | 0065-0816 | 0065-0816-02 | 1 BOTTLE, PLASTIC in 1 CARTON (0065-0816-02) / .5 mL in 1 BOTTLE, PLASTIC |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | EQ 0.7% BASE | ||||
Approval Date: | Jan 30, 2015 | TE: | RLD: | Yes | |||||
Patent: | ⤷ Try a Trial | Patent Expiration: | May 19, 2032 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
Patented Use: | TREATMENT OF OCULAR ITCHING ASSOCIATED WITH ALLERGIC CONJUNCTIVITIS | ||||||||
Patent: | ⤷ Try a Trial | Patent Expiration: | May 19, 2032 | Product Flag? | Y | Substance Flag? | Delist Request? |
Complete Access Available with Subscription