8hr arthritis pain relief

Generic: acetaminophen

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 8hr arthritis pain relief
Generic Name acetaminophen
Labeler major pharmaceuticals
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7561
Product ID 0904-7561_34388d07-02d7-72f3-e063-6294a90a6901
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215486
Listing Expiration 2026-12-31
Marketing Start 2025-05-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047561
Hyphenated Format 0904-7561

Supplemental Identifiers

RxCUI
1148399
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 8hr arthritis pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA215486 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0904-7561-60)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34388d07-02d7-72f3-e063-6294a90a6901", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["31b3aaa2-8af2-670a-e063-6394a90a8003"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0904-7561-60)", "package_ndc": "0904-7561-60", "marketing_start_date": "20250506"}], "brand_name": "8hr arthritis pain relief", "product_id": "0904-7561_34388d07-02d7-72f3-e063-6294a90a6901", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "0904-7561", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8hr arthritis pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA215486", "marketing_category": "ANDA", "marketing_start_date": "20250506", "listing_expiration_date": "20261231"}