Package 46122-170-81

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 46122-170-81
Digits Only 4612217081
Product NDC 46122-170
Description

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

Marketing

Marketing Status
Marketed Since 2002-04-30
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

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"}