nicardipine hydrochloride

Generic: nicardipine hydrochloride

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nicardipine hydrochloride
Generic Name nicardipine hydrochloride
Labeler zydus pharmaceuticals usa inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nicardipine hydrochloride 20 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-2010
Product ID 70710-2010_bf108728-380c-41b5-a730-1ddd2c0051ae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218638
Listing Expiration 2026-12-31
Marketing Start 2025-08-01

Pharmacologic Class

Classes
calcium channel antagonists [moa] cytochrome p450 2c19 inhibitors [moa] cytochrome p450 2c8 inhibitors [moa] cytochrome p450 2d6 inhibitors [moa] cytochrome p450 3a4 inhibitors [moa] dihydropyridine calcium channel blocker [epc] dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707102010
Hyphenated Format 70710-2010

Supplemental Identifiers

RxCUI
858613 858616
UPC
0370710201197
UNII
K5BC5011K3

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nicardipine hydrochloride (source: ndc)
Generic Name nicardipine hydrochloride (source: ndc)
Application Number ANDA218638 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (70710-2010-9)
source: ndc

Packages (1)

70710-2010-9 90 CAPSULE in 1 BOTTLE (70710-2010-9)

Ingredients (1)

nicardipine hydrochloride (20 mg/1)

Linked Drug Pages (1)

Nicardipine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bf108728-380c-41b5-a730-1ddd2c0051ae", "openfda": {"upc": ["0370710201197"], "unii": ["K5BC5011K3"], "rxcui": ["858613", "858616"], "spl_set_id": ["861247cc-3edf-4497-b230-2147489548b3"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (70710-2010-9)", "package_ndc": "70710-2010-9", "marketing_start_date": "20250801"}], "brand_name": "Nicardipine Hydrochloride", "product_id": "70710-2010_bf108728-380c-41b5-a730-1ddd2c0051ae", "dosage_form": "CAPSULE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 2C8 Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "70710-2010", "generic_name": "Nicardipine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nicardipine Hydrochloride", "active_ingredients": [{"name": "NICARDIPINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA218638", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}