arthritis pain acetaminophen

Generic: acetaminophen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain acetaminophen
Generic Name acetaminophen
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-673
Product ID 11673-673_13ae053f-6243-235c-e063-6394a90aa64a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215486
Listing Expiration 2026-12-31
Marketing Start 2021-12-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673673
Hyphenated Format 11673-673

Supplemental Identifiers

RxCUI
1148399
UPC
0311673673263
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 acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA215486 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (11673-673-01)
  • 1 BOTTLE in 1 CARTON (11673-673-26) / 225 TABLET in 1 BOTTLE
source: ndc

Packages (2)

11673-673-01 100 TABLET in 1 BOTTLE (11673-673-01) 11673-673-26 1 BOTTLE in 1 CARTON (11673-673-26) / 225 TABLET in 1 BOTTLE

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Arthritis Pain Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "13ae053f-6243-235c-e063-6394a90aa64a", "openfda": {"upc": ["0311673673263"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["c8025c83-77a1-c0dd-e053-2995a90a838d"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11673-673-01)", "package_ndc": "11673-673-01", "marketing_start_date": "20221130"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-673-26)  / 225 TABLET in 1 BOTTLE", "package_ndc": "11673-673-26", "marketing_start_date": "20211217"}], "brand_name": "Arthritis Pain Acetaminophen", "product_id": "11673-673_13ae053f-6243-235c-e063-6394a90aa64a", "dosage_form": "TABLET", "product_ndc": "11673-673", "generic_name": "Acetaminophen", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA215486", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}