acetaminophen
Generic: acetaminophen
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6730
Product ID
0904-6730_17f3b749-01e8-2561-e063-6294a90a5d3b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2018-09-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046730
Hyphenated Format
0904-6730
Supplemental Identifiers
RxCUI
UPC
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
- 1 BOTTLE in 1 CARTON (0904-6730-59) / 100 TABLET in 1 BOTTLE
- 100 TABLET in 1 BOTTLE (0904-6730-60)
- 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6730-61) / 10 TABLET in 1 BLISTER PACK
- 1000 TABLET in 1 BOTTLE (0904-6730-80)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "17f3b749-01e8-2561-e063-6294a90a5d3b", "openfda": {"upc": ["0309046730804"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["76cb8209-6c43-322e-e053-2991aa0a51eb"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6730-59) / 100 TABLET in 1 BOTTLE", "package_ndc": "0904-6730-59", "marketing_start_date": "20180912"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0904-6730-60)", "package_ndc": "0904-6730-60", "marketing_start_date": "20180912"}, {"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6730-61) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6730-61", "marketing_start_date": "20180912"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0904-6730-80)", "package_ndc": "0904-6730-80", "marketing_start_date": "20180912"}], "brand_name": "Acetaminophen", "product_id": "0904-6730_17f3b749-01e8-2561-e063-6294a90a5d3b", "dosage_form": "TABLET", "product_ndc": "0904-6730", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "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": "20180912", "listing_expiration_date": "20261231"}