nifedipine

Generic: nifedipine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nifedipine
Generic Name nifedipine
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

nifedipine 30 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1887
Product ID 72162-1887_fdddc45a-5ba9-42b1-9237-5f760438a3c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075269
Listing Expiration 2026-12-31
Marketing Start 2012-10-18

Pharmacologic Class

Established (EPC)
dihydropyridine calcium channel blocker [epc]
Mechanism of Action
calcium channel antagonists [moa]
Chemical Structure
dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621887
Hyphenated Format 72162-1887

Supplemental Identifiers

RxCUI
198034
UNII
I9ZF7L6G2L
NUI
N0000000069 N0000175421 M0006414

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 nifedipine (source: ndc)
Generic Name nifedipine (source: ndc)
Application Number ANDA075269 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1887-2)
source: ndc

Packages (1)

72162-1887-2 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1887-2)

Ingredients (1)

nifedipine (30 mg/1)

Linked Drug Pages (1)

Nifedipine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fdddc45a-5ba9-42b1-9237-5f760438a3c4", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034"], "spl_set_id": ["cb9d013a-2303-4e1d-a539-8ff04d5ec91d"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1887-2)", "package_ndc": "72162-1887-2", "marketing_start_date": "20241224"}], "brand_name": "Nifedipine", "product_id": "72162-1887_fdddc45a-5ba9-42b1-9237-5f760438a3c4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72162-1887", "generic_name": "Nifedipine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA075269", "marketing_category": "ANDA", "marketing_start_date": "20121018", "listing_expiration_date": "20261231"}