PLETAL - 59148-002-16 - (cilostazol)

Alphabetical Index


Drug Information of PLETAL

Product NDC: 59148-002
Proprietary Name: PLETAL
Non Proprietary Name: cilostazol
Active Ingredient(s): 100    mg/1 & nbsp;   cilostazol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PLETAL

Product NDC: 59148-002
Labeler Name: Otsuka America Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020863
Marketing Category: NDA
Start Marketing Date: 19990115

Package Information of PLETAL

Package NDC: 59148-002-16
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (59148-002-16)

NDC Information of PLETAL

NDC Code 59148-002-16
Proprietary Name PLETAL
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (59148-002-16)
Product NDC 59148-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cilostazol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990115
Marketing Category Name NDA
Labeler Name Otsuka America Pharmaceutical, Inc.
Substance Name CILOSTAZOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]

Complete Information of PLETAL


General Information