acetaminophen

Generic: acetaminophen

Labeler: walgreen co.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler walgreen co.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
WALGREEN CO.

Identifiers & Regulatory

Product NDC 0363-9604
Product ID 0363-9604_e6c2e68f-9711-4b57-b72b-ece33e19edc6
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2026-12-31
Marketing Start 2021-07-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03639604
Hyphenated Format 0363-9604

Supplemental Identifiers

RxCUI
1148399
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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 ANDA207229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-9604-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-9604-35) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e6c2e68f-9711-4b57-b72b-ece33e19edc6", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["c20d110a-ed5e-aed4-e053-2a95a90a4200"], "manufacturer_name": ["WALGREEN CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-9604-07)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "0363-9604-07", "marketing_start_date": "20210707"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-9604-35)  / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "0363-9604-35", "marketing_start_date": "20210707"}], "brand_name": "Acetaminophen", "product_id": "0363-9604_e6c2e68f-9711-4b57-b72b-ece33e19edc6", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "0363-9604", "generic_name": "Acetaminophen", "labeler_name": "WALGREEN CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207229", "marketing_category": "ANDA", "marketing_start_date": "20210707", "listing_expiration_date": "20261231"}