pain relief
Generic: acetaminophen
Labeler: aaa pharmaceutical, inc.Drug Facts
Product Profile
Brand Name
pain relief
Generic Name
acetaminophen
Labeler
aaa pharmaceutical, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57344-301
Product ID
57344-301_3b15ec5b-7738-3274-e063-6394a90a95d8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2012-12-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57344301
Hyphenated Format
57344-301
Supplemental Identifiers
RxCUI
UPC
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 (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 500 TABLET in 1 BOTTLE, PLASTIC (57344-301-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b15ec5b-7738-3274-e063-6394a90a95d8", "openfda": {"upc": ["0099581912390"], "unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["36ad21a3-6229-e91b-e063-6394a90a7933"], "manufacturer_name": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (57344-301-06)", "package_ndc": "57344-301-06", "marketing_start_date": "20250602"}], "brand_name": "Pain Relief", "product_id": "57344-301_3b15ec5b-7738-3274-e063-6394a90a95d8", "dosage_form": "TABLET", "product_ndc": "57344-301", "generic_name": "Acetaminophen", "labeler_name": "AAA Pharmaceutical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20121213", "listing_expiration_date": "20261231"}