Pharbetol - 16103-376-06 - (Acetaminophen)

Alphabetical Index


Drug Information of Pharbetol

Product NDC: 16103-376
Proprietary Name: Pharbetol
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pharbetol

Product NDC: 16103-376
Labeler Name: Pharbest Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20060110

Package Information of Pharbetol

Package NDC: 16103-376-06
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (16103-376-06) > 50 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Pharbetol

NDC Code 16103-376-06
Proprietary Name Pharbetol
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (16103-376-06) > 50 TABLET in 1 BOTTLE, PLASTIC
Product NDC 16103-376
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060110
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Pharbest Pharmaceuticals, Inc.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pharbetol


General Information