Home > National Drug Code (NDC) > PROCHLORPERAZINE MALEATE

PROCHLORPERAZINE MALEATE - 68788-6766-2 - (Prochlorperazine Maleate)

Alphabetical Index


Drug Information of PROCHLORPERAZINE MALEATE

Product NDC: 68788-6766
Proprietary Name: PROCHLORPERAZINE MALEATE
Non Proprietary Name: Prochlorperazine Maleate
Active Ingredient(s): 5    mg/1 & nbsp;   Prochlorperazine Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PROCHLORPERAZINE MALEATE

Product NDC: 68788-6766
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040268
Marketing Category: ANDA
Start Marketing Date: 20120726

Package Information of PROCHLORPERAZINE MALEATE

Package NDC: 68788-6766-2
Package Description: 20 TABLET in 1 BOTTLE (68788-6766-2)

NDC Information of PROCHLORPERAZINE MALEATE

NDC Code 68788-6766-2
Proprietary Name PROCHLORPERAZINE MALEATE
Package Description 20 TABLET in 1 BOTTLE (68788-6766-2)
Product NDC 68788-6766
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120726
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name PROCHLORPERAZINE MALEATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of PROCHLORPERAZINE MALEATE


General Information