Neoral - 0078-0248-15 - (cyclosporine)

Alphabetical Index


Drug Information of Neoral

Product NDC: 0078-0248
Proprietary Name: Neoral
Non Proprietary Name: cyclosporine
Active Ingredient(s): 100    mg/1 & nbsp;   cyclosporine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Neoral

Product NDC: 0078-0248
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050715
Marketing Category: NDA
Start Marketing Date: 19950714

Package Information of Neoral

Package NDC: 0078-0248-15
Package Description: 30 BLISTER PACK in 1 CARTON (0078-0248-15) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0078-0248-61)

NDC Information of Neoral

NDC Code 0078-0248-15
Proprietary Name Neoral
Package Description 30 BLISTER PACK in 1 CARTON (0078-0248-15) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0078-0248-61)
Product NDC 0078-0248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cyclosporine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19950714
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name CYCLOSPORINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Neoral


General Information