acetaminophen

Generic: acetaminophen

Labeler: walmart inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 650 mg/1

Manufacturer
WALMART INC.

Identifiers & Regulatory

Product NDC 79903-132
Product ID 79903-132_a3731272-35ef-4fb8-aeb2-3421f68f715a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2026-12-31
Marketing Start 2022-07-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903132
Hyphenated Format 79903-132

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
  • 325 TABLET, EXTENDED RELEASE in 1 BOTTLE (79903-132-25)
source: ndc

Packages (1)

79903-132-25 325 TABLET, EXTENDED RELEASE in 1 BOTTLE (79903-132-25)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a3731272-35ef-4fb8-aeb2-3421f68f715a", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["0035a4fd-8dd5-4534-a1b5-f510d637f721"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "325 TABLET, EXTENDED RELEASE in 1 BOTTLE (79903-132-25)", "package_ndc": "79903-132-25", "marketing_start_date": "20220726"}], "brand_name": "Acetaminophen", "product_id": "79903-132_a3731272-35ef-4fb8-aeb2-3421f68f715a", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "79903-132", "generic_name": "Acetaminophen", "labeler_name": "WALMART INC.", "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": "20220726", "listing_expiration_date": "20261231"}