pharbetol regular strength

Generic: acetaminophen

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pharbetol regular strength
Generic Name acetaminophen
Labeler atlantic biologicals corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0353
Product ID 17856-0353_36d8e8fb-3928-ffbe-e063-6394a90a5779
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2007-01-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560353
Hyphenated Format 17856-0353

Supplemental Identifiers

RxCUI
313782 1298830
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 regular strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX, UNIT-DOSE (17856-0353-1) / 1 TABLET in 1 POUCH (17856-0353-2)
  • 24 TABLET in 1 BOTTLE (17856-0353-4)
source: ndc

Packages (2)

17856-0353-1 100 POUCH in 1 BOX, UNIT-DOSE (17856-0353-1) / 1 TABLET in 1 POUCH (17856-0353-2) 17856-0353-4 24 TABLET in 1 BOTTLE (17856-0353-4)

Ingredients (1)

acetaminophen (325 mg/1)

Linked Drug Pages (1)

Pharbetol Regular strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "36d8e8fb-3928-ffbe-e063-6394a90a5779", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782", "1298830"], "spl_set_id": ["05a91d24-b498-4ba2-a275-68b871cf62d2"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (17856-0353-1)  / 1 TABLET in 1 POUCH (17856-0353-2)", "package_ndc": "17856-0353-1", "marketing_start_date": "20240626"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (17856-0353-4)", "package_ndc": "17856-0353-4", "marketing_start_date": "20240626"}], "brand_name": "Pharbetol Regular strength", "product_id": "17856-0353_36d8e8fb-3928-ffbe-e063-6394a90a5779", "dosage_form": "TABLET", "product_ndc": "17856-0353", "generic_name": "Acetaminophen", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pharbetol", "brand_name_suffix": "Regular strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20070109", "listing_expiration_date": "20261231"}