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RISPERDAL M-TAB - 50458-395-30 - (risperidone)

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Drug Information of RISPERDAL M-TAB

Product NDC: 50458-395
Proprietary Name: RISPERDAL M-TAB
Non Proprietary Name: risperidone
Active Ingredient(s): .5    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERDAL M-TAB

Product NDC: 50458-395
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021444
Marketing Category: NDA
Start Marketing Date: 20030402

Package Information of RISPERDAL M-TAB

Package NDC: 50458-395-30
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50458-395-30)

NDC Information of RISPERDAL M-TAB

NDC Code 50458-395-30
Proprietary Name RISPERDAL M-TAB
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50458-395-30)
Product NDC 50458-395
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20030402
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name RISPERIDONE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERDAL M-TAB


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