niacor

Generic: niacin

Labeler: avondale pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name niacor
Generic Name niacin
Labeler avondale pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

niacin 500 mg/1

Manufacturer
Avondale Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 71740-001
Product ID 71740-001_800ff22d-b10c-4cc8-920f-217a4d23563d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040378
Listing Expiration 2026-12-31
Marketing Start 2000-05-03

Pharmacologic Class

Established (EPC)
nicotinic acid [epc]
Chemical Structure
nicotinic acids [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71740001
Hyphenated Format 71740-001

Supplemental Identifiers

RxCUI
198024 311944
UNII
2679MF687A
NUI
N0000175594 M0014839

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 niacor (source: ndc)
Generic Name niacin (source: ndc)
Application Number ANDA040378 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71740-001-10)
source: ndc

Packages (1)

Ingredients (1)

niacin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "800ff22d-b10c-4cc8-920f-217a4d23563d", "openfda": {"nui": ["N0000175594", "M0014839"], "unii": ["2679MF687A"], "rxcui": ["198024", "311944"], "spl_set_id": ["bf287412-160b-403f-8eb4-57f29a475902"], "pharm_class_cs": ["Nicotinic Acids [CS]"], "pharm_class_epc": ["Nicotinic Acid [EPC]"], "manufacturer_name": ["Avondale Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71740-001-10)", "package_ndc": "71740-001-10", "marketing_start_date": "20211216"}], "brand_name": "Niacor", "product_id": "71740-001_800ff22d-b10c-4cc8-920f-217a4d23563d", "dosage_form": "TABLET", "pharm_class": ["Nicotinic Acid [EPC]", "Nicotinic Acids [CS]"], "product_ndc": "71740-001", "generic_name": "Niacin", "labeler_name": "Avondale Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Niacor", "active_ingredients": [{"name": "NIACIN", "strength": "500 mg/1"}], "application_number": "ANDA040378", "marketing_category": "ANDA", "marketing_start_date": "20000503", "listing_expiration_date": "20261231"}