good sense pain relief arthritis pain

Generic: acetaminophen

Labeler: asclemed usa inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name good sense pain relief arthritis pain
Generic Name acetaminophen
Labeler asclemed usa inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
ASCLEMED USA INC.

Identifiers & Regulatory

Product NDC 76420-590
Product ID 76420-590_3886c8f2-b1c3-4da9-e063-6394a90a956e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075077
Listing Expiration 2026-12-31
Marketing Start 2005-11-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420590
Hyphenated Format 76420-590

Supplemental Identifiers

RxCUI
1148399
UNII
362O9ITL9D

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 good sense pain relief 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
  • 1 BOTTLE in 1 CARTON (76420-590-01) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-60)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-90)
source: ndc

Packages (4)

76420-590-01 1 BOTTLE in 1 CARTON (76420-590-01) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE 76420-590-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-30) 76420-590-60 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-60) 76420-590-90 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-90)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

good sense pain relief arthritis pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3886c8f2-b1c3-4da9-e063-6394a90a956e", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["2315ec07-e5b8-4332-8bc2-4e28e88892f3"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (76420-590-01)  / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "76420-590-01", "marketing_start_date": "20250626"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-30)", "package_ndc": "76420-590-30", "marketing_start_date": "20250626"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-60)", "package_ndc": "76420-590-60", "marketing_start_date": "20250626"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-90)", "package_ndc": "76420-590-90", "marketing_start_date": "20250626"}], "brand_name": "good sense pain relief arthritis pain", "product_id": "76420-590_3886c8f2-b1c3-4da9-e063-6394a90a956e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "76420-590", "generic_name": "Acetaminophen", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "good sense pain relief", "brand_name_suffix": "arthritis pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20051121", "listing_expiration_date": "20261231"}