Details for New Drug Application (NDA): 208105
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The generic ingredient in DESIPRAMINE HYDROCHLORIDE is desipramine hydrochloride. There are nine drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the desipramine hydrochloride profile page.
Summary for 208105
Tradename: | DESIPRAMINE HYDROCHLORIDE |
Applicant: | Amneal Pharms Co |
Ingredient: | desipramine hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 208105
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DESIPRAMINE HYDROCHLORIDE | desipramine hydrochloride | TABLET;ORAL | 208105 | ANDA | Amneal Pharmaceuticals NY LLC | 69238-1053 | 69238-1053-1 | 100 TABLET, FILM COATED in 1 BOTTLE (69238-1053-1) |
DESIPRAMINE HYDROCHLORIDE | desipramine hydrochloride | TABLET;ORAL | 208105 | ANDA | Amneal Pharmaceuticals NY LLC | 69238-1053 | 69238-1053-3 | 30 TABLET, FILM COATED in 1 BOTTLE (69238-1053-3) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Mar 17, 2016 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Mar 17, 2016 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Mar 17, 2016 | TE: | AB | RLD: | No |
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