MAXALT-MLT - 54868-4499-0 - (rizatriptan benzoate)

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Drug Information of MAXALT-MLT

Product NDC: 54868-4499
Proprietary Name: MAXALT-MLT
Non Proprietary Name: rizatriptan benzoate
Active Ingredient(s): 10    mg/1 & nbsp;   rizatriptan benzoate
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of MAXALT-MLT

Product NDC: 54868-4499
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020865
Marketing Category: NDA
Start Marketing Date: 20091229

Package Information of MAXALT-MLT

Package NDC: 54868-4499-0
Package Description: 3 POUCH in 1 CONTAINER (54868-4499-0) > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of MAXALT-MLT

NDC Code 54868-4499-0
Proprietary Name MAXALT-MLT
Package Description 3 POUCH in 1 CONTAINER (54868-4499-0) > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 54868-4499
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rizatriptan benzoate
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20091229
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name RIZATRIPTAN BENZOATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of MAXALT-MLT


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