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Prochlorperazine Maleate - 55289-568-20 - (prochlorperazine maleate)

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Drug Information of Prochlorperazine Maleate

Product NDC: 55289-568
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Prochlorperazine Maleate

Product NDC: 55289-568
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040185
Marketing Category: ANDA
Start Marketing Date: 20101213

Package Information of Prochlorperazine Maleate

Package NDC: 55289-568-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-568-20)

NDC Information of Prochlorperazine Maleate

NDC Code 55289-568-20
Proprietary Name Prochlorperazine Maleate
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-568-20)
Product NDC 55289-568
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prochlorperazine maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101213
Marketing Category Name ANDA
Labeler Name PD-Rx 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


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