acetaminophen

Generic: acetaminophen

Labeler: better living brands, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler better living brands, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Better Living Brands, LLC

Identifiers & Regulatory

Product NDC 21130-108
Product ID 21130-108_3cc99dcb-b853-48bb-95bb-41a14cf78711
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2026-12-31
Marketing Start 2022-06-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130108
Hyphenated Format 21130-108

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 (21130-108-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-108-35) / 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": "3cc99dcb-b853-48bb-95bb-41a14cf78711", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["de3d9840-4ada-5c9a-e053-2a95a90a5721"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-108-07)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "21130-108-07", "marketing_start_date": "20220624"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-108-35)  / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "21130-108-35", "marketing_start_date": "20220624"}], "brand_name": "Acetaminophen", "product_id": "21130-108_3cc99dcb-b853-48bb-95bb-41a14cf78711", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "21130-108", "generic_name": "Acetaminophen", "labeler_name": "Better Living Brands, LLC", "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": "20220624", "listing_expiration_date": "20261231"}