Details for New Drug Application (NDA): 072879
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The generic ingredient in AMOXAPINE is amoxapine. There are four drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the amoxapine profile page.
Summary for 072879
Tradename: | AMOXAPINE |
Applicant: | Chartwell Rx |
Ingredient: | amoxapine |
Patents: | 0 |
Suppliers and Packaging for NDA: 072879
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
AMOXAPINE | amoxapine | TABLET;ORAL | 072879 | ANDA | Chartwell RX, LLC | 62135-703 | 62135-703-30 | 30 TABLET in 1 BOTTLE (62135-703-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 150MG | ||||
Approval Date: | Jun 28, 1991 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Jun 28, 1991 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Jun 28, 1991 | TE: | RLD: | No |
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