pain relief

Generic: acetaminophen

Labeler: aaa pharmaceutical, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name acetaminophen
Labeler aaa pharmaceutical, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1

Manufacturer
AAA Pharmaceutical, Inc.

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
313782
UPC
0099581912390
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE, PLASTIC (57344-301-06)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (325 mg/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"}