Package 69396-144-01
Brand: acetaminophen
Generic: acetaminophenPackage Facts
Identity
Package NDC
69396-144-01
Digits Only
6939614401
Product NDC
69396-144
Description
1000 TABLET in 1 BOTTLE (69396-144-01)
Marketing
Marketing Status
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": "09935a81-941d-1499-e063-6294a90a049c", "openfda": {"upc": ["0860004834403"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["09935a74-34b0-0e7c-e063-6294a90a7c83"], "manufacturer_name": ["Trifecta Pharmaceuticals USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (69396-144-01)", "package_ndc": "69396-144-01", "marketing_start_date": "20231107"}], "brand_name": "Acetaminophen", "product_id": "69396-144_09935a81-941d-1499-e063-6294a90a049c", "dosage_form": "TABLET", "product_ndc": "69396-144", "generic_name": "Acetaminophen", "labeler_name": "Trifecta Pharmaceuticals USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230808", "listing_expiration_date": "20261231"}