acetaminophen
Generic: acetaminophen
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
aurohealth llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 160 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-774
Product ID
58602-774_0b45ff6e-f4aa-ffdd-e063-6394a90ab825
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2022-06-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602774
Hyphenated Format
58602-774
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
- 160 mg/1
Packaging
- 8 BLISTER PACK in 1 CARTON (58602-774-82) / 6 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b45ff6e-f4aa-ffdd-e063-6394a90ab825", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313820"], "spl_set_id": ["30756257-f748-4a5d-b031-dd267d0f91ad"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 BLISTER PACK in 1 CARTON (58602-774-82) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-774-82", "marketing_start_date": "20220618"}], "brand_name": "Acetaminophen", "product_id": "58602-774_0b45ff6e-f4aa-ffdd-e063-6394a90ab825", "dosage_form": "TABLET", "product_ndc": "58602-774", "generic_name": "Acetaminophen", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220618", "listing_expiration_date": "20261231"}