arthritis pain reliever

Generic: acetaminophen

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain reliever
Generic Name acetaminophen
Labeler walgreen company
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0544
Product ID 0363-0544_14730300-066e-40c6-bf1a-55993ad3b185
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075077
Listing Expiration 2026-12-31
Marketing Start 2000-05-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630544
Hyphenated Format 0363-0544

Supplemental Identifiers

RxCUI
1148399
UPC
0311917180014
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 reliever (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
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0544-78)
source: ndc

Packages (1)

0363-0544-78 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0544-78)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

arthritis pain reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14730300-066e-40c6-bf1a-55993ad3b185", "openfda": {"upc": ["0311917180014"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["5028c116-d0e3-4e30-8fa8-caaf08d99ec7"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0544-78)", "package_ndc": "0363-0544-78", "marketing_start_date": "20140731"}], "brand_name": "arthritis pain reliever", "product_id": "0363-0544_14730300-066e-40c6-bf1a-55993ad3b185", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "0363-0544", "generic_name": "Acetaminophen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "arthritis pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20000526", "listing_expiration_date": "20261231"}