niacin

Generic: niacin

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

Drug Facts

Product Profile

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

niacin 500 mg/1

Manufacturer
Redmont Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 71741-020
Product ID 71741-020_984e26b5-be06-4b88-b13b-7488fcb46516
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 71741020
Hyphenated Format 71741-020

Supplemental Identifiers

RxCUI
198024
UPC
0371741020603
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 niacin (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
  • 30 TABLET in 1 BOTTLE (71741-020-30)
  • 60 TABLET in 1 BOTTLE (71741-020-60)
  • 90 TABLET in 1 BOTTLE (71741-020-90)
source: ndc

Packages (3)

Ingredients (1)

niacin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "984e26b5-be06-4b88-b13b-7488fcb46516", "openfda": {"nui": ["N0000175594", "M0014839"], "upc": ["0371741020603"], "unii": ["2679MF687A"], "rxcui": ["198024"], "spl_set_id": ["f51f7e6d-b132-48d8-8bb1-54203472f0d8"], "pharm_class_cs": ["Nicotinic Acids [CS]"], "pharm_class_epc": ["Nicotinic Acid [EPC]"], "manufacturer_name": ["Redmont Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71741-020-30)", "package_ndc": "71741-020-30", "marketing_start_date": "20251212"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71741-020-60)", "package_ndc": "71741-020-60", "marketing_start_date": "20251212"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71741-020-90)", "package_ndc": "71741-020-90", "marketing_start_date": "20211216"}], "brand_name": "Niacin", "product_id": "71741-020_984e26b5-be06-4b88-b13b-7488fcb46516", "dosage_form": "TABLET", "pharm_class": ["Nicotinic Acid [EPC]", "Nicotinic Acids [CS]"], "product_ndc": "71741-020", "generic_name": "Niacin", "labeler_name": "Redmont Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Niacin", "active_ingredients": [{"name": "NIACIN", "strength": "500 mg/1"}], "application_number": "ANDA040378", "marketing_category": "ANDA", "marketing_start_date": "20000503", "listing_expiration_date": "20261231"}