RESTORIL - 0406-9917-01 - (temazepam)

Alphabetical Index


Drug Information of RESTORIL

Product NDC: 0406-9917
Proprietary Name: RESTORIL
Non Proprietary Name: temazepam
Active Ingredient(s): 30    mg/1 & nbsp;   temazepam
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of RESTORIL

Product NDC: 0406-9917
Labeler Name: Mallinckrodt, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018163
Marketing Category: NDA
Start Marketing Date: 20110707

Package Information of RESTORIL

Package NDC: 0406-9917-01
Package Description: 100 CAPSULE in 1 BOTTLE (0406-9917-01)

NDC Information of RESTORIL

NDC Code 0406-9917-01
Proprietary Name RESTORIL
Package Description 100 CAPSULE in 1 BOTTLE (0406-9917-01)
Product NDC 0406-9917
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110707
Marketing Category Name NDA
Labeler Name Mallinckrodt, Inc.
Substance Name TEMAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of RESTORIL


General Information