Details for New Drug Application (NDA): 090175
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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-eight suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride profile page.
Summary for 090175
Tradename: | DONEPEZIL HYDROCHLORIDE |
Applicant: | Zydus Pharms Usa Inc |
Ingredient: | donepezil hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 090175
Mechanism of Action | Cholinesterase Inhibitors |
Suppliers and Packaging for NDA: 090175
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET, ORALLY DISINTEGRATING;ORAL | 090175 | ANDA | Zydus Lifesciences Limited | 65841-721 | 65841-721-01 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-01) |
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET, ORALLY DISINTEGRATING;ORAL | 090175 | ANDA | Zydus Lifesciences Limited | 65841-721 | 65841-721-05 | 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 5MG | ||||
Approval Date: | May 10, 2011 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 10MG | ||||
Approval Date: | May 10, 2011 | TE: | RLD: | No |
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