Home > National Drug Code (NDC) > Meclizine Hydrochloride

Meclizine Hydrochloride - 53808-0380-1 - (MECLIZINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Meclizine Hydrochloride

Product NDC: 53808-0380
Proprietary Name: Meclizine Hydrochloride
Non Proprietary Name: MECLIZINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   MECLIZINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meclizine Hydrochloride

Product NDC: 53808-0380
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087128
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Meclizine Hydrochloride

Package NDC: 53808-0380-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0380-1)

NDC Information of Meclizine Hydrochloride

NDC Code 53808-0380-1
Proprietary Name Meclizine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (53808-0380-1)
Product NDC 53808-0380
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MECLIZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antiemetic [EPC],Emesis Suppression [PE]

Complete Information of Meclizine Hydrochloride


General Information