duralgina
Generic: acetaminophen
Labeler: menper distributors inc.Drug Facts
Product Profile
Brand Name
duralgina
Generic Name
acetaminophen
Labeler
menper distributors inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
53145-013
Product ID
53145-013_3a893b13-e7ee-c5b1-e063-6394a90a4253
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2027-12-31
Marketing Start
2017-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53145013
Hyphenated Format
53145-013
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
duralgina (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (53145-013-71)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a893b13-e7ee-c5b1-e063-6394a90a4253", "openfda": {"upc": ["0042279108056"], "unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["bb31f66c-80a9-4bdb-983b-cef5d21de5ff"], "manufacturer_name": ["Menper Distributors Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (53145-013-71)", "package_ndc": "53145-013-71", "marketing_start_date": "20170101"}], "brand_name": "Duralgina", "product_id": "53145-013_3a893b13-e7ee-c5b1-e063-6394a90a4253", "dosage_form": "TABLET", "product_ndc": "53145-013", "generic_name": "Acetaminophen", "labeler_name": "Menper Distributors Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Duralgina", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170101", "listing_expiration_date": "20271231"}