Details for New Drug Application (NDA): 078662
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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-seven suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride profile page.
Summary for 078662
Tradename: | DONEPEZIL HYDROCHLORIDE |
Applicant: | Strides Pharma |
Ingredient: | donepezil hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 078662
Mechanism of Action | Cholinesterase Inhibitors |
Suppliers and Packaging for NDA: 078662
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET;ORAL | 078662 | ANDA | Coupler LLC | 67046-1467 | 67046-1467-3 | 30 TABLET in 1 BLISTER PACK (67046-1467-3) |
DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride | TABLET;ORAL | 078662 | ANDA | Preferred Pharmaceuticals Inc. | 68788-8711 | 68788-8711-3 | 30 TABLET in 1 BOTTLE (68788-8711-3) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | May 31, 2011 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | May 31, 2011 | TE: | AB | RLD: | No |
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