Temazepam - 51079-419-20 - (temazepam)

Alphabetical Index


Drug Information of Temazepam

Product NDC: 51079-419
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: 51079-419
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070920
Marketing Category: ANDA
Start Marketing Date: 20110204

Package Information of Temazepam

Package NDC: 51079-419-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-419-20) > 1 CAPSULE in 1 BLISTER PACK (51079-419-01)

NDC Information of Temazepam

NDC Code 51079-419-20
Proprietary Name Temazepam
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-419-20) > 1 CAPSULE in 1 BLISTER PACK (51079-419-01)
Product NDC 51079-419
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110204
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name TEMAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Temazepam


General Information