nicardipine hydrochloride

Generic: nicardipine hydrochloride

Labeler: puracap laboratories llc dba blu pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nicardipine hydrochloride
Generic Name nicardipine hydrochloride
Labeler puracap laboratories llc dba blu pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nicardipine hydrochloride 20 mg/1

Manufacturer
PuraCap Laboratories LLC dba Blu Pharmaceuticals

Identifiers & Regulatory

Product NDC 24658-750
Product ID 24658-750_69c60be8-143d-4a50-8a66-46c01c416372
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074928
Listing Expiration 2026-12-31
Marketing Start 2016-12-15

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 24658750
Hyphenated Format 24658-750

Supplemental Identifiers

RxCUI
858613 858616
UPC
0324658750903 0324658751900
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 ANDA074928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (24658-750-90)
source: ndc

Packages (1)

24658-750-90 90 CAPSULE in 1 BOTTLE (24658-750-90)

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": "69c60be8-143d-4a50-8a66-46c01c416372", "openfda": {"upc": ["0324658750903", "0324658751900"], "unii": ["K5BC5011K3"], "rxcui": ["858613", "858616"], "spl_set_id": ["065efabf-8c7d-4dd5-aef2-700c2eca399d"], "manufacturer_name": ["PuraCap Laboratories LLC dba Blu Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (24658-750-90)", "package_ndc": "24658-750-90", "marketing_start_date": "20161215"}], "brand_name": "Nicardipine Hydrochloride", "product_id": "24658-750_69c60be8-143d-4a50-8a66-46c01c416372", "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": "24658-750", "generic_name": "Nicardipine Hydrochloride", "labeler_name": "PuraCap Laboratories LLC dba Blu Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nicardipine Hydrochloride", "active_ingredients": [{"name": "NICARDIPINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA074928", "marketing_category": "ANDA", "marketing_start_date": "20161215", "listing_expiration_date": "20261231"}