arthritis pain relief

Generic: acetaminophen

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain relief
Generic Name acetaminophen
Labeler topco associates llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
TOPCO ASSOCIATES LLC

Identifiers & Regulatory

Product NDC 36800-632
Product ID 36800-632_ea392a2b-465a-6a66-e053-2a95a90a62c8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2022-10-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36800632
Hyphenated Format 36800-632

Supplemental Identifiers

RxCUI
1148399
UPC
0036800106178
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
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-01) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
  • 150 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (36800-632-05)
source: ndc

Packages (4)

36800-632-01 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-01) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC 36800-632-02 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC 36800-632-03 1 BOTTLE, PLASTIC in 1 CARTON (36800-632-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC 36800-632-05 150 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (36800-632-05)

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": "ea392a2b-465a-6a66-e053-2a95a90a62c8", "openfda": {"upc": ["0036800106178"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["e60aa992-f5f7-3506-e053-2995a90a7abd"], "manufacturer_name": ["TOPCO ASSOCIATES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-632-01)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "36800-632-01", "marketing_start_date": "20221004"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-632-02)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "36800-632-02", "marketing_start_date": "20221004"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-632-03)  / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "36800-632-03", "marketing_start_date": "20221004"}, {"sample": false, "description": "150 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (36800-632-05)", "package_ndc": "36800-632-05", "marketing_start_date": "20221004"}], "brand_name": "Arthritis Pain Relief", "product_id": "36800-632_ea392a2b-465a-6a66-e053-2a95a90a62c8", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "36800-632", "generic_name": "Acetaminophen", "labeler_name": "TOPCO ASSOCIATES LLC", "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_start_date": "20221004", "listing_expiration_date": "20261231"}