Alahist - 50991-607-15 - (Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of Alahist

Product NDC: 50991-607
Proprietary Name: Alahist
Non Proprietary Name: Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride
Active Ingredient(s): 25; 7.5    mg/5mL; mg/5mL & nbsp;   Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Alahist

Product NDC: 50991-607
Labeler Name: Poly Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20071220

Package Information of Alahist

Package NDC: 50991-607-15
Package Description: 12 BOTTLE in 1 TRAY (50991-607-15) > 15 mL in 1 BOTTLE

NDC Information of Alahist

NDC Code 50991-607-15
Proprietary Name Alahist
Package Description 12 BOTTLE in 1 TRAY (50991-607-15) > 15 mL in 1 BOTTLE
Product NDC 50991-607
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20071220
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Poly Pharmaceuticals, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 25; 7.5
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Alahist


General Information