acetaminophen extra strength

Generic: acetaminophen

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Cardinal Health 110, LLC. DBA Leader

Identifiers & Regulatory

Product NDC 70000-0312
Product ID 70000-0312_2fba5924-6bc0-42d8-84e1-1c581ca2be3a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2004-05-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000312
Hyphenated Format 70000-0312

Supplemental Identifiers

RxCUI
198440
UPC
0096295132335
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 extra strength (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 (70000-0312-1) / 50 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (70000-0312-2) / 100 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (2)

70000-0312-1 1 BOTTLE in 1 CARTON (70000-0312-1) / 50 TABLET, COATED in 1 BOTTLE 70000-0312-2 1 BOTTLE in 1 CARTON (70000-0312-2) / 100 TABLET, COATED in 1 BOTTLE

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2fba5924-6bc0-42d8-84e1-1c581ca2be3a", "openfda": {"upc": ["0096295132335"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["dd8b13a5-07df-4cec-92c3-1a662b1e1a56"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0312-1)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "70000-0312-1", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0312-2)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "70000-0312-2", "marketing_start_date": "20040510"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "70000-0312_2fba5924-6bc0-42d8-84e1-1c581ca2be3a", "dosage_form": "TABLET, COATED", "product_ndc": "70000-0312", "generic_name": "Acetaminophen", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20271231"}