Dallergy - 16477-160-01 - (CHLORCYCLIZINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Dallergy

Product NDC: 16477-160
Proprietary Name: Dallergy
Non Proprietary Name: CHLORCYCLIZINE HYDROCHLORIDE
Active Ingredient(s): 25; 10    mg/1; mg/1 & nbsp;   CHLORCYCLIZINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dallergy

Product NDC: 16477-160
Labeler Name: Laser Pharmaceuticals, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111101

Package Information of Dallergy

Package NDC: 16477-160-01
Package Description: 100 TABLET in 1 BOTTLE (16477-160-01)

NDC Information of Dallergy

NDC Code 16477-160-01
Proprietary Name Dallergy
Package Description 100 TABLET in 1 BOTTLE (16477-160-01)
Product NDC 16477-160
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CHLORCYCLIZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Laser Pharmaceuticals, LLC
Substance Name CHLORCYCLIZINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 25; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Dallergy


General Information