Details for New Drug Application (NDA): 218638
✉ Email this page to a colleague
The generic ingredient in NICARDIPINE HYDROCHLORIDE is nicardipine hydrochloride. There are eleven drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the nicardipine hydrochloride profile page.
Summary for 218638
| Tradename: | NICARDIPINE HYDROCHLORIDE |
| Applicant: | Navinta Llc |
| Ingredient: | nicardipine hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 218638
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | CAPSULE;ORAL | 218638 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-2010 | 70710-2010-9 | 90 CAPSULE in 1 BOTTLE (70710-2010-9) |
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | CAPSULE;ORAL | 218638 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-2011 | 70710-2011-9 | 90 CAPSULE in 1 BOTTLE (70710-2011-9) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 20MG | ||||
| Approval Date: | Jun 25, 2025 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 30MG | ||||
| Approval Date: | Jun 25, 2025 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
