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Prochlorperazine - 54868-3112-1 - (Prochlorperazine)

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Drug Information of Prochlorperazine

Product NDC: 54868-3112
Proprietary Name: Prochlorperazine
Non Proprietary Name: Prochlorperazine
Active Ingredient(s): 25    mg/1 & nbsp;   Prochlorperazine
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Prochlorperazine

Product NDC: 54868-3112
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040058
Marketing Category: ANDA
Start Marketing Date: 20010720

Package Information of Prochlorperazine

Package NDC: 54868-3112-1
Package Description: 6 SUPPOSITORY in 1 BOTTLE, PLASTIC (54868-3112-1)

NDC Information of Prochlorperazine

NDC Code 54868-3112-1
Proprietary Name Prochlorperazine
Package Description 6 SUPPOSITORY in 1 BOTTLE, PLASTIC (54868-3112-1)
Product NDC 54868-3112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 20010720
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROCHLORPERAZINE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Prochlorperazine


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