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Prochlorperazine Maleate - 49349-148-02 - (Prochlorperazine Maleate)

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Drug Information of Prochlorperazine Maleate

Product NDC: 49349-148
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: 49349-148
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040120
Marketing Category: ANDA
Start Marketing Date: 20110411

Package Information of Prochlorperazine Maleate

Package NDC: 49349-148-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-148-02)

NDC Information of Prochlorperazine Maleate

NDC Code 49349-148-02
Proprietary Name Prochlorperazine Maleate
Package Description 30 TABLET in 1 BLISTER PACK (49349-148-02)
Product NDC 49349-148
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prochlorperazine Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110411
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PROCHLORPERAZINE MALEATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Prochlorperazine Maleate


General Information