Details for New Drug Application (NDA): 077745
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The generic ingredient in QUETIAPINE FUMARATE is quetiapine fumarate. There are fifty-three drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the quetiapine fumarate profile page.
Summary for 077745
Tradename: | QUETIAPINE FUMARATE |
Applicant: | Teva Pharms |
Ingredient: | quetiapine fumarate |
Patents: | 0 |
Suppliers and Packaging for NDA: 077745
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
QUETIAPINE FUMARATE | quetiapine fumarate | TABLET;ORAL | 077745 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-2063 | 0093-2063-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-2063-01) |
QUETIAPINE FUMARATE | quetiapine fumarate | TABLET;ORAL | 077745 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-8162 | 0093-8162-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-8162-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 25MG BASE | ||||
Approval Date: | Mar 27, 2012 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | Mar 27, 2012 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 100MG BASE | ||||
Approval Date: | Mar 27, 2012 | TE: | AB | RLD: | No |
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