ZALEPLON - 63629-3906-3 - (ZALEPLON)

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Drug Information of ZALEPLON

Product NDC: 63629-3906
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: 63629-3906
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020859
Marketing Category: NDA
Start Marketing Date: 20080501

Package Information of ZALEPLON

Package NDC: 63629-3906-3
Package Description: 90 CAPSULE in 1 BOTTLE (63629-3906-3)

NDC Information of ZALEPLON

NDC Code 63629-3906-3
Proprietary Name ZALEPLON
Package Description 90 CAPSULE in 1 BOTTLE (63629-3906-3)
Product NDC 63629-3906
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 Bryant Ranch Prepack
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


General Information