extra strength acetaminophen

Generic: acetaminophen

Labeler: cvs pharmacy, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength acetaminophen
Generic Name acetaminophen
Labeler cvs pharmacy, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
CVS PHARMACY, INC.

Identifiers & Regulatory

Product NDC 69842-390
Product ID 69842-390_8e71c727-66ab-497b-ad8e-0230b43f9a1d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 2017-11-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842390
Hyphenated Format 69842-390

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 extra strength acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 15 POUCH in 1 CARTON (69842-390-54) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e71c727-66ab-497b-ad8e-0230b43f9a1d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["3f9c230b-e6ea-4786-992b-9c7204425209"], "manufacturer_name": ["CVS PHARMACY, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 POUCH in 1 CARTON (69842-390-54)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "69842-390-54", "marketing_start_date": "20171109"}], "brand_name": "Extra Strength Acetaminophen", "product_id": "69842-390_8e71c727-66ab-497b-ad8e-0230b43f9a1d", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69842-390", "generic_name": "Acetaminophen", "labeler_name": "CVS PHARMACY, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20171109", "listing_expiration_date": "20261231"}