acetaminophen
Generic: acetaminophen
Labeler: walgreen co.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
walgreen co.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 160 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-9605
Product ID
0363-9605_0bfa94dc-1f27-efa5-e063-6394a90aa629
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2021-07-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03639605
Hyphenated Format
0363-9605
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
- 4 BLISTER PACK in 1 CARTON (0363-9605-07) / 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": "0bfa94dc-1f27-efa5-e063-6394a90aa629", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313820"], "spl_set_id": ["c20c814b-35f5-4c46-e053-2a95a90a50f2"], "manufacturer_name": ["WALGREEN CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-9605-07) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "0363-9605-07", "marketing_start_date": "20210705"}], "brand_name": "Acetaminophen", "product_id": "0363-9605_0bfa94dc-1f27-efa5-e063-6394a90aa629", "dosage_form": "TABLET", "product_ndc": "0363-9605", "generic_name": "Acetaminophen", "labeler_name": "WALGREEN CO.", "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": "20210705", "listing_expiration_date": "20261231"}