Package 79903-032-40

Brand: extra strength acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 79903-032-40
Digits Only 7990303240
Product NDC 79903-032
Description

1 BOTTLE in 1 CARTON (79903-032-40) / 40 TABLET in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2029-04-30
Brand extra strength acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "495e1164-7604-42c2-e063-6394a90aa96d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["a88eba4c-0701-4eec-9a24-a804186fbfd8"], "manufacturer_name": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (79903-032-02)  / 100 TABLET in 1 BOTTLE (79903-032-01)", "package_ndc": "79903-032-02", "marketing_end_date": "20280930", "marketing_start_date": "20210112"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (79903-032-10)", "package_ndc": "79903-032-10", "marketing_start_date": "20210112"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-032-40)  / 40 TABLET in 1 BOTTLE", "package_ndc": "79903-032-40", "marketing_end_date": "20290430", "marketing_start_date": "20210112"}], "brand_name": "EXTRA STRENGTH ACETAMINOPHEN", "product_id": "79903-032_495e1164-7604-42c2-e063-6394a90aa96d", "dosage_form": "TABLET", "product_ndc": "79903-032", "generic_name": "ACETAMINOPHEN", "labeler_name": "Wal-Mart Stores Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210105", "listing_expiration_date": "20271231"}