acetaminophen
Generic: acetaminophen
Labeler: aphena pharma solutions - tennessee, llcDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
aphena pharma solutions - tennessee, llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71610-238
Product ID
71610-238_a14457be-2ebb-46db-96dd-ebceb51c077f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH NOT FINAL
Application Number
part343
Listing Expiration
2026-12-31
Marketing Start
2015-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71610238
Hyphenated Format
71610-238
Supplemental Identifiers
RxCUI
UNII
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
acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
part343 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (71610-238-65)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a14457be-2ebb-46db-96dd-ebceb51c077f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["89134c3e-ec5b-4a57-952a-98d6c6cff7c2"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71610-238-65)", "package_ndc": "71610-238-65", "marketing_start_date": "20190213"}], "brand_name": "Acetaminophen", "product_id": "71610-238_a14457be-2ebb-46db-96dd-ebceb51c077f", "dosage_form": "TABLET", "product_ndc": "71610-238", "generic_name": "Acetaminophen", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20150501", "listing_expiration_date": "20261231"}