acetaminophen
Generic: acetaminophen
Labeler: sam's west incDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
sam's west inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68196-177
Product ID
68196-177_46538673-56ff-e1fd-e063-6394a90a5052
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-02-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68196177
Hyphenated Format
68196-177
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
- 600 TABLET in 1 BOTTLE (68196-177-61)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46538673-56ff-e1fd-e063-6394a90a5052", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0c8e7095-0806-4501-e063-6394a90a89aa"], "manufacturer_name": ["SAM'S WEST INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET in 1 BOTTLE (68196-177-61)", "package_ndc": "68196-177-61", "marketing_start_date": "20240213"}], "brand_name": "Acetaminophen", "product_id": "68196-177_46538673-56ff-e1fd-e063-6394a90a5052", "dosage_form": "TABLET", "product_ndc": "68196-177", "generic_name": "Acetaminophen", "labeler_name": "SAM'S WEST 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": "20240213", "listing_expiration_date": "20261231"}