pain relief extra strength
Generic: acetaminophen
Labeler: chain drug marketing association, inc.Drug Facts
Product Profile
Brand Name
pain relief extra strength
Generic Name
acetaminophen
Labeler
chain drug marketing association, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83324-078
Product ID
83324-078_458b4f7d-8f0c-2559-e063-6294a90a663b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-04-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83324078
Hyphenated Format
83324-078
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
pain relief extra strength (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-078-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
- 500 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-05)
- 150 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-15)
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-078-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-078-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (5)
83324-078-01
1 BOTTLE, PLASTIC in 1 CARTON (83324-078-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
83324-078-05
500 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-05)
83324-078-15
150 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-15)
83324-078-24
1 BOTTLE, PLASTIC in 1 CARTON (83324-078-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
83324-078-50
1 BOTTLE, PLASTIC in 1 CARTON (83324-078-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458b4f7d-8f0c-2559-e063-6294a90a663b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c57c10fc-f182-4153-8974-ef359a5f5ac1"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-078-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-078-01", "marketing_start_date": "20240403"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-05)", "package_ndc": "83324-078-05", "marketing_start_date": "20240403"}, {"sample": false, "description": "150 TABLET, COATED in 1 BOTTLE, PLASTIC (83324-078-15)", "package_ndc": "83324-078-15", "marketing_start_date": "20240403"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-078-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-078-24", "marketing_start_date": "20240403"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-078-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-078-50", "marketing_start_date": "20240403"}], "brand_name": "Pain Relief Extra Strength", "product_id": "83324-078_458b4f7d-8f0c-2559-e063-6294a90a663b", "dosage_form": "TABLET, COATED", "product_ndc": "83324-078", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240403", "listing_expiration_date": "20261231"}