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Risperidone - 55111-470-81 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 55111-470
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): 3    mg/1 & nbsp;   Risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 55111-470
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077328
Marketing Category: ANDA
Start Marketing Date: 20091130

Package Information of Risperidone

Package NDC: 55111-470-81
Package Description: 3 BLISTER PACK in 1 CARTON (55111-470-81) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Risperidone

NDC Code 55111-470-81
Proprietary Name Risperidone
Package Description 3 BLISTER PACK in 1 CARTON (55111-470-81) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 55111-470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20091130
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name RISPERIDONE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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