acetaminophen
Generic: acetaminophen
Labeler: cvs health corpDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cvs health corp
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-968
Product ID
69842-968_2e010044-3dee-3a65-e063-6294a90a65a9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2021-04-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842968
Hyphenated Format
69842-968
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (69842-968-01) / 100 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e010044-3dee-3a65-e063-6294a90a65a9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["bbc48c9e-7eb8-2c67-e053-2a95a90a8552"], "manufacturer_name": ["CVS HEALTH CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-968-01) / 100 TABLET in 1 BOTTLE", "package_ndc": "69842-968-01", "marketing_start_date": "20210410"}], "brand_name": "ACETAMINOPHEN", "product_id": "69842-968_2e010044-3dee-3a65-e063-6294a90a65a9", "dosage_form": "TABLET", "product_ndc": "69842-968", "generic_name": "ACETAMINOPHEN", "labeler_name": "CVS HEALTH CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210410", "listing_expiration_date": "20261231"}