Package 37835-507-01

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37835-507-01
Digits Only 3783550701
Product NDC 37835-507
Description

100 TABLET in 1 BOTTLE (37835-507-01)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "371d5ff5-bfe9-1a6f-e063-6294a90a3b19", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["35483db0-d6b8-4b37-8113-1dbe51e42ae5"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37835-507-01)", "package_ndc": "37835-507-01", "marketing_start_date": "20250501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (37835-507-05)", "package_ndc": "37835-507-05", "marketing_start_date": "20250501"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (37835-507-25)", "package_ndc": "37835-507-25", "marketing_start_date": "20250501"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "37835-507_371d5ff5-bfe9-1a6f-e063-6294a90a3b19", "dosage_form": "TABLET", "product_ndc": "37835-507", "generic_name": "Acetaminophen", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}