Temazepam - 0781-2202-01 - (Temazepam)

Alphabetical Index


Drug Information of Temazepam

Product NDC: 0781-2202
Proprietary Name: Temazepam
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 Temazepam

Product NDC: 0781-2202
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071428
Marketing Category: ANDA
Start Marketing Date: 19880112

Package Information of Temazepam

Package NDC: 0781-2202-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2202-01)

NDC Information of Temazepam

NDC Code 0781-2202-01
Proprietary Name Temazepam
Package Description 100 CAPSULE in 1 BOTTLE (0781-2202-01)
Product NDC 0781-2202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19880112
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name TEMAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Temazepam


General Information