temazepam - 67877-146-01 - (temazepam)

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Drug Information of temazepam

Product NDC: 67877-146
Proprietary Name: temazepam
Non Proprietary Name: temazepam
Active Ingredient(s): 15    mg/1 & nbsp;   temazepam
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of temazepam

Product NDC: 67877-146
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071456
Marketing Category: ANDA
Start Marketing Date: 19870421

Package Information of temazepam

Package NDC: 67877-146-01
Package Description: 100 CAPSULE in 1 BOTTLE (67877-146-01)

NDC Information of temazepam

NDC Code 67877-146-01
Proprietary Name temazepam
Package Description 100 CAPSULE in 1 BOTTLE (67877-146-01)
Product NDC 67877-146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19870421
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
Substance Name TEMAZEPAM
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of temazepam


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