rapidol
Generic: acetaminophen
Labeler: pharmadel llcDrug Facts
Product Profile
Brand Name
rapidol
Generic Name
acetaminophen
Labeler
pharmadel llc
Dosage Form
CAPSULE, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55758-503
Product ID
55758-503_3b2aeccc-ae65-c8fc-e063-6294a90a32f7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-07-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55758503
Hyphenated Format
55758-503
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
rapidol (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55758-503-24) / 24 CAPSULE, COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}