Details for New Drug Application (NDA): 219608
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The generic ingredient in NICARDIPINE HYDROCHLORIDE is nicardipine hydrochloride. There are eleven drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the nicardipine hydrochloride profile page.
Summary for 219608
| Tradename: | NICARDIPINE HYDROCHLORIDE |
| Applicant: | Qilu Pharm Hainan |
| Ingredient: | nicardipine hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 219608
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | INJECTABLE;INJECTION | 219608 | ANDA | Sagent Pharmaceuticals | 25021-333 | 25021-333-10 | 10 VIAL in 1 CARTON (25021-333-10) / 10 mL in 1 VIAL |
| NICARDIPINE HYDROCHLORIDE | nicardipine hydrochloride | INJECTABLE;INJECTION | 219608 | ANDA | Qilu Pharmaceutical Co., Ltd. | 67184-0611 | 67184-0611-2 | 10 VIAL in 1 CARTON (67184-0611-2) / 10 mL in 1 VIAL (67184-0611-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 25MG/10ML (2.5MG/ML) | ||||
| Approval Date: | Oct 28, 2025 | TE: | AP | RLD: | No | ||||
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