8 hour arthritis pain

Generic: acetaminophen

Labeler: chain drug marketing association, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 8 hour arthritis pain
Generic Name acetaminophen
Labeler chain drug marketing association, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION, INC.

Identifiers & Regulatory

Product NDC 83324-083
Product ID 83324-083_1ac70227-c7d7-de60-e063-6394a90aeed7
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2024-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324083
Hyphenated Format 83324-083

Supplemental Identifiers

RxCUI
1148399
UPC
0635515954984
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 hour arthritis pain (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA211544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83324-083-01)
  • 1 BOTTLE, PLASTIC in 1 CARTON (83324-083-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

83324-083-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83324-083-01) 83324-083-50 1 BOTTLE, PLASTIC in 1 CARTON (83324-083-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

8 Hour Arthritis Pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1ac70227-c7d7-de60-e063-6394a90aeed7", "openfda": {"upc": ["0635515954984"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b098ebf6-a76d-4550-b5c4-fdc3b4ceb9a8"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83324-083-01)", "package_ndc": "83324-083-01", "marketing_start_date": "20240501"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-083-50)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "83324-083-50", "marketing_start_date": "20240501"}], "brand_name": "8 Hour Arthritis Pain", "product_id": "83324-083_1ac70227-c7d7-de60-e063-6394a90aeed7", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "83324-083", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8 Hour Arthritis Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}