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PROCHLORPERAZINE MALEATE - 66336-921-30 - (Prochlorperazine maleate)

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Drug Information of PROCHLORPERAZINE MALEATE

Product NDC: 66336-921
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
Coding System: National Drug Codes(NDC)

Labeler Information of PROCHLORPERAZINE MALEATE

Product NDC: 66336-921
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040268
Marketing Category: ANDA
Start Marketing Date: 19980301

Package Information of PROCHLORPERAZINE MALEATE

Package NDC: 66336-921-30
Package Description: 30 TABLET in 1 BOTTLE (66336-921-30)

NDC Information of PROCHLORPERAZINE MALEATE

NDC Code 66336-921-30
Proprietary Name PROCHLORPERAZINE MALEATE
Package Description 30 TABLET in 1 BOTTLE (66336-921-30)
Product NDC 66336-921
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980301
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
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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