temazepam - 67877-149-30 - (temazepam)

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Drug Information of temazepam

Product NDC: 67877-149
Proprietary Name: temazepam
Non Proprietary Name: temazepam
Active Ingredient(s): 22.5    mg/1 & nbsp;   temazepam
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of temazepam

Product NDC: 67877-149
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071457
Marketing Category: ANDA
Start Marketing Date: 20120628

Package Information of temazepam

Package NDC: 67877-149-30
Package Description: 30 CAPSULE in 1 BOTTLE (67877-149-30)

NDC Information of temazepam

NDC Code 67877-149-30
Proprietary Name temazepam
Package Description 30 CAPSULE in 1 BOTTLE (67877-149-30)
Product NDC 67877-149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120628
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
Substance Name TEMAZEPAM
Strength Number 22.5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of temazepam


General Information