arthritis pain relief

Generic: acetaminophen

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain relief
Generic Name acetaminophen
Labeler chain drug consortium
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
CHAIN DRUG CONSORTIUM

Identifiers & Regulatory

Product NDC 68016-303
Product ID 68016-303_243426e7-9529-c46a-e063-6394a90a9341
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Marketing Start 2020-08-01
Marketing End 2026-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68016303
Hyphenated Format 68016-303

Supplemental Identifiers

RxCUI
1148399
UPC
0840986036897
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 arthritis pain relief (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 (68016-303-01)
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-303-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

68016-303-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68016-303-01) 68016-303-50 1 BOTTLE, PLASTIC in 1 CARTON (68016-303-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Arthritis Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "243426e7-9529-c46a-e063-6394a90a9341", "openfda": {"upc": ["0840986036897"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["778a15d5-3fa4-4386-8afb-751f4537c10d"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68016-303-01)", "package_ndc": "68016-303-01", "marketing_end_date": "20260930", "marketing_start_date": "20200801"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-303-50)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "68016-303-50", "marketing_end_date": "20260630", "marketing_start_date": "20200801"}], "brand_name": "Arthritis Pain Relief", "product_id": "68016-303_243426e7-9529-c46a-e063-6394a90a9341", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "68016-303", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20200801"}