acetaminophen

Generic: acetaminophen

Labeler: retail business services,llc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler retail business services,llc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
RETAIL BUSINESS SERVICES,LLC.

Identifiers & Regulatory

Product NDC 72476-185
Product ID 72476-185_4651bbcf-6529-2fb3-e063-6294a90a0e8f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2020-08-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72476185
Hyphenated Format 72476-185

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 ANDA211544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-05)
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-10)
  • 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-21)
source: ndc

Packages (3)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4651bbcf-6529-2fb3-e063-6294a90a0e8f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["a0fb0afe-9c25-d0f6-e053-2995a90adbba"], "manufacturer_name": ["RETAIL BUSINESS SERVICES,LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-05)", "package_ndc": "72476-185-05", "marketing_start_date": "20200819"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-10)", "package_ndc": "72476-185-10", "marketing_start_date": "20200819"}, {"sample": false, "description": "225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72476-185-21)", "package_ndc": "72476-185-21", "marketing_start_date": "20200819"}], "brand_name": "Acetaminophen", "product_id": "72476-185_4651bbcf-6529-2fb3-e063-6294a90a0e8f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "72476-185", "generic_name": "Acetaminophen", "labeler_name": "RETAIL BUSINESS SERVICES,LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20200819", "listing_expiration_date": "20261231"}