8 hr arthritis pain

Generic: acetaminophen

Labeler: cvs woonsocket prescription center, incorporated
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 8 hr arthritis pain
Generic Name acetaminophen
Labeler cvs woonsocket prescription center, incorporated
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Identifiers & Regulatory

Product NDC 51316-504
Product ID 51316-504_429c1da2-954d-412d-9065-bb67ebbdf3aa
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075077
Listing Expiration 2026-12-31
Marketing Start 2025-09-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51316504
Hyphenated Format 51316-504

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 8 hr arthritis pain (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA075077 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51316-504-79)
  • 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51316-504-83)
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": "429c1da2-954d-412d-9065-bb67ebbdf3aa", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["68e5b8a7-17ca-4a29-9f0c-7350fcf65928"], "manufacturer_name": ["CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51316-504-79)", "package_ndc": "51316-504-79", "marketing_start_date": "20250929"}, {"sample": false, "description": "225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51316-504-83)", "package_ndc": "51316-504-83", "marketing_start_date": "20250929"}], "brand_name": "8 hr arthritis pain", "product_id": "51316-504_429c1da2-954d-412d-9065-bb67ebbdf3aa", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "51316-504", "generic_name": "acetaminophen", "labeler_name": "CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8 hr arthritis pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}