Home > National Drug Code (NDC) > Poly Hist PD

Poly Hist PD - 50991-222-45 - (Thonzylamine Hydrochloride and Chlophedianol Hydrochloride)

Alphabetical Index


Drug Information of Poly Hist PD

Product NDC: 50991-222
Proprietary Name: Poly Hist PD
Non Proprietary Name: Thonzylamine Hydrochloride and Chlophedianol Hydrochloride
Active Ingredient(s): 6.25; 6.25    mg/mL; mg/mL & nbsp;   Thonzylamine Hydrochloride and Chlophedianol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Poly Hist PD

Product NDC: 50991-222
Labeler Name: Poly Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130701

Package Information of Poly Hist PD

Package NDC: 50991-222-45
Package Description: 45 mL in 1 BOTTLE (50991-222-45)

NDC Information of Poly Hist PD

NDC Code 50991-222-45
Proprietary Name Poly Hist PD
Package Description 45 mL in 1 BOTTLE (50991-222-45)
Product NDC 50991-222
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Thonzylamine Hydrochloride and Chlophedianol Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Poly Pharmaceuticals, Inc.
Substance Name CHLOPHEDIANOL HYDROCHLORIDE; THONZYLAMINE HYDROCHLORIDE
Strength Number 6.25; 6.25
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Poly Hist PD


General Information