Bonine - 63736-044-12 - (Chlorcyclizine Hydrochloride)

Alphabetical Index


Drug Information of Bonine

Product NDC: 63736-044
Proprietary Name: Bonine
Non Proprietary Name: Chlorcyclizine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Chlorcyclizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Bonine

Product NDC: 63736-044
Labeler Name: Insight Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090608

Package Information of Bonine

Package NDC: 63736-044-12
Package Description: 12 TABLET, CHEWABLE in 1 BOX (63736-044-12)

NDC Information of Bonine

NDC Code 63736-044-12
Proprietary Name Bonine
Package Description 12 TABLET, CHEWABLE in 1 BOX (63736-044-12)
Product NDC 63736-044
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorcyclizine Hydrochloride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20090608
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Insight Pharmaceuticals
Substance Name CHLORCYCLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bonine


General Information