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Risperidone - 49884-212-55 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 49884-212
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): .25    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: 49884-212
Labeler Name: Par Pharmaceutical Companies, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077494
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Risperidone

Package NDC: 49884-212-55
Package Description: 5 BLISTER PACK in 1 CARTON (49884-212-55) > 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-212-52)

NDC Information of Risperidone

NDC Code 49884-212-55
Proprietary Name Risperidone
Package Description 5 BLISTER PACK in 1 CARTON (49884-212-55) > 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-212-52)
Product NDC 49884-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Companies, Inc.
Substance Name RISPERIDONE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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