Zaleplon - 0378-6810-10 - (Zaleplon)

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Drug Information of Zaleplon

Product NDC: 0378-6810
Proprietary Name: Zaleplon
Non Proprietary Name: Zaleplon
Active Ingredient(s): 10    mg/1 & nbsp;   Zaleplon
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zaleplon

Product NDC: 0378-6810
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077238
Marketing Category: ANDA
Start Marketing Date: 20120501

Package Information of Zaleplon

Package NDC: 0378-6810-10
Package Description: 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-6810-10)

NDC Information of Zaleplon

NDC Code 0378-6810-10
Proprietary Name Zaleplon
Package Description 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-6810-10)
Product NDC 0378-6810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zaleplon
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120501
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ZALEPLON
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes gamma-Aminobutyric Acid A Receptor Agonist [EPC],GABA A Agonists [MoA],Central Nervous System Depression [PE]

Complete Information of Zaleplon


General Information