ZALEPLON - 21695-376-60 - (ZALEPLON)

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Drug Information of ZALEPLON

Product NDC: 21695-376
Proprietary Name: ZALEPLON
Non Proprietary Name: ZALEPLON
Active Ingredient(s): 5    mg/1 & nbsp;   ZALEPLON
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ZALEPLON

Product NDC: 21695-376
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020859
Marketing Category: NDA
Start Marketing Date: 20080501

Package Information of ZALEPLON

Package NDC: 21695-376-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (21695-376-60)

NDC Information of ZALEPLON

NDC Code 21695-376-60
Proprietary Name ZALEPLON
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (21695-376-60)
Product NDC 21695-376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ZALEPLON
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080501
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
Substance Name ZALEPLON
Strength Number 5
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


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