Home > National Drug Code (NDC) > Promethazine Hydrochloride

Promethazine Hydrochloride - 10702-002-01 - (Promethazine Hydrochloride)

Alphabetical Index


Drug Information of Promethazine Hydrochloride

Product NDC: 10702-002
Proprietary Name: Promethazine Hydrochloride
Non Proprietary Name: Promethazine Hydrochloride
Active Ingredient(s): 12.5    mg/1 & nbsp;   Promethazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine Hydrochloride

Product NDC: 10702-002
Labeler Name: KVK-Tech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040712
Marketing Category: ANDA
Start Marketing Date: 20120717

Package Information of Promethazine Hydrochloride

Package NDC: 10702-002-01
Package Description: 100 TABLET in 1 BOTTLE (10702-002-01)

NDC Information of Promethazine Hydrochloride

NDC Code 10702-002-01
Proprietary Name Promethazine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (10702-002-01)
Product NDC 10702-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120717
Marketing Category Name ANDA
Labeler Name KVK-Tech, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine Hydrochloride


General Information