Cilostazol - 0185-0223-05 - (Cilostazol)

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Drug Information of Cilostazol

Product NDC: 0185-0223
Proprietary Name: Cilostazol
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 Cilostazol

Product NDC: 0185-0223
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077021
Marketing Category: ANDA
Start Marketing Date: 20041123

Package Information of Cilostazol

Package NDC: 0185-0223-05
Package Description: 500 TABLET in 1 BOTTLE (0185-0223-05)

NDC Information of Cilostazol

NDC Code 0185-0223-05
Proprietary Name Cilostazol
Package Description 500 TABLET in 1 BOTTLE (0185-0223-05)
Product NDC 0185-0223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cilostazol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041123
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name CILOSTAZOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]

Complete Information of Cilostazol


General Information