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Prochlorperazine Maleate - 63629-1335-1 - (Prochlorperazine Maleate)

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Drug Information of Prochlorperazine Maleate

Product NDC: 63629-1335
Proprietary Name: Prochlorperazine Maleate
Non Proprietary Name: Prochlorperazine Maleate
Active Ingredient(s): 10    mg/1 & nbsp;   Prochlorperazine Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Prochlorperazine Maleate

Product NDC: 63629-1335
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040120
Marketing Category: ANDA
Start Marketing Date: 19960725

Package Information of Prochlorperazine Maleate

Package NDC: 63629-1335-1
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (63629-1335-1)

NDC Information of Prochlorperazine Maleate

NDC Code 63629-1335-1
Proprietary Name Prochlorperazine Maleate
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (63629-1335-1)
Product NDC 63629-1335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine Maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19960725
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name PROCHLORPERAZINE MALEATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Prochlorperazine Maleate


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