Details for New Drug Application (NDA): 203656
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The generic ingredient in DONEPEZIL HYDROCHLORIDE is donepezil hydrochloride. There are thirty-two drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride profile page.
Summary for 203656
Tradename: | DONEPEZIL HYDROCHLORIDE |
Applicant: | Unichem |
Ingredient: | donepezil hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 203656
Mechanism of Action | Cholinesterase Inhibitors |
Suppliers and Packaging for NDA: 203656
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET;ORAL | 203656 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-248 | 29300-248-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-248-01) |
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET;ORAL | 203656 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-248 | 29300-248-10 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-248-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Jun 23, 2016 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Jun 23, 2016 | TE: | RLD: | No |
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