acetaminophen
Generic: acetaminophen
Labeler: cvs pharmacy, incDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cvs pharmacy, inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51316-177
Product ID
51316-177_46545d0f-6657-d84a-e063-6394a90a2028
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-11-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316177
Hyphenated Format
51316-177
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
- 500 mg/1
Packaging
- 150 TABLET in 1 BOTTLE (51316-177-15)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46545d0f-6657-d84a-e063-6394a90a2028", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["1ddb8a2b-3081-3eda-e063-6294a90ab82b"], "manufacturer_name": ["CVS PHARMACY, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 BOTTLE (51316-177-15)", "package_ndc": "51316-177-15", "marketing_start_date": "20241126"}], "brand_name": "Acetaminophen", "product_id": "51316-177_46545d0f-6657-d84a-e063-6394a90a2028", "dosage_form": "TABLET", "product_ndc": "51316-177", "generic_name": "Acetaminophen", "labeler_name": "CVS PHARMACY, INC", "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": "20241126", "listing_expiration_date": "20261231"}