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Prochlorperazine Edisylate - 54868-0261-0 - (Prochlorperazine Edisylate)

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Drug Information of Prochlorperazine Edisylate

Product NDC: 54868-0261
Proprietary Name: Prochlorperazine Edisylate
Non Proprietary Name: Prochlorperazine Edisylate
Active Ingredient(s): 5    mg/mL & nbsp;   Prochlorperazine Edisylate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Prochlorperazine Edisylate

Product NDC: 54868-0261
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040540
Marketing Category: ANDA
Start Marketing Date: 20040726

Package Information of Prochlorperazine Edisylate

Package NDC: 54868-0261-0
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (54868-0261-0) > 10 mL in 1 VIAL

NDC Information of Prochlorperazine Edisylate

NDC Code 54868-0261-0
Proprietary Name Prochlorperazine Edisylate
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (54868-0261-0) > 10 mL in 1 VIAL
Product NDC 54868-0261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine Edisylate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20040726
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROCHLORPERAZINE EDISYLATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Prochlorperazine Edisylate


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