Zaleplon - 16714-551-02 - (Zaleplon)

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Drug Information of Zaleplon

Product NDC: 16714-551
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: 16714-551
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090374
Marketing Category: ANDA
Start Marketing Date: 20100623

Package Information of Zaleplon

Package NDC: 16714-551-02
Package Description: 100 CAPSULE in 1 BOTTLE (16714-551-02)

NDC Information of Zaleplon

NDC Code 16714-551-02
Proprietary Name Zaleplon
Package Description 100 CAPSULE in 1 BOTTLE (16714-551-02)
Product NDC 16714-551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zaleplon
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100623
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
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