acetaminophen

Generic: acetaminophen

Labeler: amerisource bergen
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler amerisource bergen
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Amerisource Bergen

Identifiers & Regulatory

Product NDC 46122-170
Product ID 46122-170_c7cc85d7-e528-4cdc-8550-7e431c10c3a5
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076200
Listing Expiration 2026-12-31
Marketing Start 2002-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46122170
Hyphenated Format 46122-170

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 ANDA076200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-170-81)
source: ndc

Packages (1)

46122-170-81 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-170-81)

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": "c7cc85d7-e528-4cdc-8550-7e431c10c3a5", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["71be6a5b-aff2-4757-804a-085b44e2a7d3"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-170-81)", "package_ndc": "46122-170-81", "marketing_start_date": "20020430"}], "brand_name": "Acetaminophen", "product_id": "46122-170_c7cc85d7-e528-4cdc-8550-7e431c10c3a5", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "46122-170", "generic_name": "Acetaminophen", "labeler_name": "Amerisource Bergen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA076200", "marketing_category": "ANDA", "marketing_start_date": "20020430", "listing_expiration_date": "20261231"}