acetaminophen

Generic: acetaminophen

Labeler: health pharma usa llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler health pharma usa llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1

Manufacturer
Health Pharma USA LLC

Identifiers & Regulatory

Product NDC 71679-305
Product ID 71679-305_3f74fbae-e3af-1f3e-e063-6394a90a644c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2025-09-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71679305
Hyphenated Format 71679-305

Supplemental Identifiers

RxCUI
313782
UNII
362O9ITL9D

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 acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 47000 TABLET, FILM COATED in 1 DRUM (71679-305-00)
source: ndc

Packages (1)

71679-305-00 47000 TABLET, FILM COATED in 1 DRUM (71679-305-00)

Ingredients (1)

acetaminophen (325 mg/1)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f74fbae-e3af-1f3e-e063-6394a90a644c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["671adabe-5f82-4599-a133-3f67ccb34079"], "manufacturer_name": ["Health Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "47000 TABLET, FILM COATED in 1 DRUM (71679-305-00)", "package_ndc": "71679-305-00", "marketing_start_date": "20250923"}], "brand_name": "Acetaminophen", "product_id": "71679-305_3f74fbae-e3af-1f3e-e063-6394a90a644c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71679-305", "generic_name": "Acetaminophen", "labeler_name": "Health Pharma USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}