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Prochlorperazine Maleate - 54868-1082-2 - (Prochlorperazine Maleate)

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Drug Information of Prochlorperazine Maleate

Product NDC: 54868-1082
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: 54868-1082
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040101
Marketing Category: ANDA
Start Marketing Date: 20000107

Package Information of Prochlorperazine Maleate

Package NDC: 54868-1082-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-1082-2)

NDC Information of Prochlorperazine Maleate

NDC Code 54868-1082-2
Proprietary Name Prochlorperazine Maleate
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-1082-2)
Product NDC 54868-1082
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine Maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000107
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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