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Prochlorperazine Maleate - 55154-5094-0 - (prochlorperazine maleate)

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Drug Information of Prochlorperazine Maleate

Product NDC: 55154-5094
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: 55154-5094
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040185
Marketing Category: ANDA
Start Marketing Date: 20110128

Package Information of Prochlorperazine Maleate

Package NDC: 55154-5094-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5094-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Prochlorperazine Maleate

NDC Code 55154-5094-0
Proprietary Name Prochlorperazine Maleate
Package Description 10 BLISTER PACK in 1 BAG (55154-5094-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5094
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prochlorperazine maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110128
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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