Details for New Drug Application (NDA): 074670
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The generic ingredient in NICARDIPINE HYDROCHLORIDE is nicardipine hydrochloride. There are eleven drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the nicardipine hydrochloride profile page.
Summary for 074670
Tradename: | NICARDIPINE HYDROCHLORIDE |
Applicant: | Ani Pharms |
Ingredient: | nicardipine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 074670
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | CAPSULE;ORAL | 074670 | ANDA | ANI Pharmaceuticals, Inc. | 62559-205 | 62559-205-90 | 90 CAPSULE in 1 BOTTLE (62559-205-90) |
NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | CAPSULE;ORAL | 074670 | ANDA | ANI Pharmaceuticals, Inc. | 62559-206 | 62559-206-90 | 90 CAPSULE in 1 BOTTLE (62559-206-90) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 20MG | ||||
Approval Date: | Oct 28, 1996 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 30MG | ||||
Approval Date: | Oct 28, 1996 | TE: | AB | RLD: | No |
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