acetaminophen - apap arthritis

Generic: acetaminophen

Labeler: valu merchandisers company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen - apap arthritis
Generic Name acetaminophen
Labeler valu merchandisers company
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Valu Merchandisers Company

Identifiers & Regulatory

Product NDC 63941-333
Product ID 63941-333_2a405453-5fb1-3502-e063-6394a90ae41a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076200
Listing Expiration 2026-12-31
Marketing Start 2002-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63941333
Hyphenated Format 63941-333

Supplemental Identifiers

RxCUI
1148399
UPC
0070038610892
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 - apap arthritis (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA076200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63941-333-01)
  • 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63941-333-50)
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a405453-5fb1-3502-e063-6394a90ae41a", "openfda": {"upc": ["0070038610892"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["793a6fa6-4ff0-498f-ae1b-71bcafb1fd73"], "manufacturer_name": ["Valu Merchandisers Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63941-333-01)", "package_ndc": "63941-333-01", "marketing_start_date": "20020430"}, {"sample": false, "description": "50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63941-333-50)", "package_ndc": "63941-333-50", "marketing_start_date": "20020430"}], "brand_name": "Acetaminophen - APAP Arthritis", "product_id": "63941-333_2a405453-5fb1-3502-e063-6394a90ae41a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "63941-333", "generic_name": "Acetaminophen", "labeler_name": "Valu Merchandisers Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen - APAP Arthritis", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA076200", "marketing_category": "ANDA", "marketing_start_date": "20020430", "listing_expiration_date": "20261231"}