Package 71679-305-00

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71679-305-00
Digits Only 7167930500
Product NDC 71679-305
Product ID 71679-305_3f74fbae-e3af-1f3e-e063-6394a90a644c
Description

47000 TABLET, FILM COATED in 1 DRUM (71679-305-00)

Marketing

Marketing Status
Marketed Since 2025-09-23
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f74fbae-e3af-1f3e-e063-6394a90a644c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["671adabe-5f82-4599-a133-3f67ccb34079"], "manufacturer_name": ["Health Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "47000 TABLET, FILM COATED in 1 DRUM (71679-305-00)", "package_ndc": "71679-305-00", "marketing_start_date": "20250923"}], "brand_name": "Acetaminophen", "product_id": "71679-305_3f74fbae-e3af-1f3e-e063-6394a90a644c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71679-305", "generic_name": "Acetaminophen", "labeler_name": "Health Pharma USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}