Nimodipine - 55154-4560-0 - (Nimodipine)

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Drug Information of Nimodipine

Product NDC: 55154-4560
Proprietary Name: Nimodipine
Non Proprietary Name: Nimodipine
Active Ingredient(s): 30    mg/1 & nbsp;   Nimodipine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nimodipine

Product NDC: 55154-4560
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077067
Marketing Category: ANDA
Start Marketing Date: 20070628

Package Information of Nimodipine

Package NDC: 55154-4560-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4560-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Nimodipine

NDC Code 55154-4560-0
Proprietary Name Nimodipine
Package Description 10 BLISTER PACK in 1 BAG (55154-4560-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-4560
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nimodipine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070628
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name NIMODIPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nimodipine


General Information