acetaminophen
Generic: acetaminophen
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
nucare pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3959
Product ID
68071-3959_49660efe-1322-6942-e063-6294a90a0686
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2027-12-31
Marketing Start
2022-02-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713959
Hyphenated Format
68071-3959
Supplemental Identifiers
RxCUI
UPC
UNII
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
- 1 BOTTLE in 1 CARTON (68071-3959-1) / 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": "49660efe-1322-6942-e063-6294a90a0686", "openfda": {"upc": ["0368071395914"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["4965fc33-f815-d49e-e063-6394a90a119c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68071-3959-1) / 100 TABLET in 1 BOTTLE", "package_ndc": "68071-3959-1", "marketing_start_date": "20260127"}], "brand_name": "ACETAMINOPHEN", "product_id": "68071-3959_49660efe-1322-6942-e063-6294a90a0686", "dosage_form": "TABLET", "product_ndc": "68071-3959", "generic_name": "ACETAMINOPHEN", "labeler_name": "NuCare Pharmaceuticals, 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": "20220215", "listing_expiration_date": "20271231"}