Package 55758-503-24

Brand: rapidol

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 55758-503-24
Digits Only 5575850324
Product NDC 55758-503
Description

1 BOTTLE in 1 CARTON (55758-503-24) / 24 CAPSULE, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-07-17
Brand rapidol
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b2aeccc-ae65-c8fc-e063-6294a90a32f7", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198439"], "spl_set_id": ["3a210860-1fc1-e496-e063-6394a90a8705"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55758-503-24)  / 24 CAPSULE, COATED in 1 BOTTLE", "package_ndc": "55758-503-24", "marketing_start_date": "20250717"}], "brand_name": "Rapidol", "product_id": "55758-503_3b2aeccc-ae65-c8fc-e063-6294a90a32f7", "dosage_form": "CAPSULE, COATED", "product_ndc": "55758-503", "generic_name": "ACETAMINOPHEN", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rapidol", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250717", "listing_expiration_date": "20261231"}