acetaminophen

Generic: acetaminophen

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6720
Product ID 0904-6720_9cb0e7d2-6c42-4c46-a557-e495d7ccb05d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2018-07-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046720
Hyphenated Format 0904-6720

Supplemental Identifiers

RxCUI
198440
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 acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0904-6720-24) / 24 TABLET in 1 BOTTLE
  • 500 TABLET in 1 BOTTLE (0904-6720-40)
  • 1 BOTTLE in 1 CARTON (0904-6720-51) / 50 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0904-6720-59) / 100 TABLET in 1 BOTTLE
  • 100 TABLET in 1 BOTTLE (0904-6720-60)
  • 1000 TABLET in 1 BOTTLE (0904-6720-80)
source: ndc

Packages (6)

0904-6720-24 1 BOTTLE in 1 CARTON (0904-6720-24) / 24 TABLET in 1 BOTTLE 0904-6720-40 500 TABLET in 1 BOTTLE (0904-6720-40) 0904-6720-51 1 BOTTLE in 1 CARTON (0904-6720-51) / 50 TABLET in 1 BOTTLE 0904-6720-59 1 BOTTLE in 1 CARTON (0904-6720-59) / 100 TABLET in 1 BOTTLE 0904-6720-60 100 TABLET in 1 BOTTLE (0904-6720-60) 0904-6720-80 1000 TABLET in 1 BOTTLE (0904-6720-80)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9cb0e7d2-6c42-4c46-a557-e495d7ccb05d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["020fa486-31f0-4e0c-84d3-5b3aaded1eeb"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6720-24)  / 24 TABLET in 1 BOTTLE", "package_ndc": "0904-6720-24", "marketing_start_date": "20180828"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0904-6720-40)", "package_ndc": "0904-6720-40", "marketing_start_date": "20180828"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6720-51)  / 50 TABLET in 1 BOTTLE", "package_ndc": "0904-6720-51", "marketing_start_date": "20180730"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6720-59)  / 100 TABLET in 1 BOTTLE", "package_ndc": "0904-6720-59", "marketing_start_date": "20180730"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0904-6720-60)", "package_ndc": "0904-6720-60", "marketing_start_date": "20180827"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0904-6720-80)", "package_ndc": "0904-6720-80", "marketing_start_date": "20180726"}], "brand_name": "acetaminophen", "product_id": "0904-6720_9cb0e7d2-6c42-4c46-a557-e495d7ccb05d", "dosage_form": "TABLET", "product_ndc": "0904-6720", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180726", "listing_expiration_date": "20271231"}