Details for New Drug Application (NDA): 208781
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The generic ingredient in QUETIAPINE FUMARATE is quetiapine fumarate. There are fifty-three drug master file entries for this compound. Fifty suppliers are listed for this compound. Additional details are available on the quetiapine fumarate profile page.
Summary for 208781
Tradename: | QUETIAPINE FUMARATE |
Applicant: | Prinston Inc |
Ingredient: | quetiapine fumarate |
Patents: | 0 |
Suppliers and Packaging for NDA: 208781
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
QUETIAPINE FUMARATE | quetiapine fumarate | TABLET, EXTENDED RELEASE;ORAL | 208781 | ANDA | Solco Healthcare U.S., LLC | 43547-019 | 43547-019-06 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-019-06) |
QUETIAPINE FUMARATE | quetiapine fumarate | TABLET, EXTENDED RELEASE;ORAL | 208781 | ANDA | Solco Healthcare U.S., LLC | 43547-019 | 43547-019-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-019-50) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | Apr 26, 2022 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 150MG BASE | ||||
Approval Date: | Apr 26, 2022 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 200MG BASE | ||||
Approval Date: | Apr 26, 2022 | TE: | AB | RLD: | No |
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