pharbetol

Generic: acetaminophen

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pharbetol
Generic Name acetaminophen
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-478
Product ID 71205-478_27ee285e-c641-4364-bd4a-7273b8e0cad2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2006-01-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205478
Hyphenated Format 71205-478

Supplemental Identifiers

RxCUI
198440 1293942
UPC
0371205478506
UNII
362O9ITL9D

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 pharbetol (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (71205-478-20)
  • 24 TABLET in 1 BOTTLE, PLASTIC (71205-478-24)
  • 30 TABLET in 1 BOTTLE, PLASTIC (71205-478-30)
  • 40 TABLET in 1 BOTTLE, PLASTIC (71205-478-40)
  • 50 TABLET in 1 BOTTLE, PLASTIC (71205-478-50)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71205-478-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71205-478-90)
source: ndc

Packages (7)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27ee285e-c641-4364-bd4a-7273b8e0cad2", "openfda": {"upc": ["0371205478506"], "unii": ["362O9ITL9D"], "rxcui": ["198440", "1293942"], "spl_set_id": ["51ba690e-d76b-41c6-a083-8bc803e1faa2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (71205-478-20)", "package_ndc": "71205-478-20", "marketing_start_date": "20240126"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE, PLASTIC (71205-478-24)", "package_ndc": "71205-478-24", "marketing_start_date": "20200930"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71205-478-30)", "package_ndc": "71205-478-30", "marketing_start_date": "20200930"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (71205-478-40)", "package_ndc": "71205-478-40", "marketing_start_date": "20201012"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (71205-478-50)", "package_ndc": "71205-478-50", "marketing_start_date": "20201012"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-478-60)", "package_ndc": "71205-478-60", "marketing_start_date": "20200930"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-478-90)", "package_ndc": "71205-478-90", "marketing_start_date": "20200930"}], "brand_name": "Pharbetol", "product_id": "71205-478_27ee285e-c641-4364-bd4a-7273b8e0cad2", "dosage_form": "TABLET", "product_ndc": "71205-478", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pharbetol", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060110", "listing_expiration_date": "20261231"}