temazepam - 63629-1621-2 - (temazepam)

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Drug Information of temazepam

Product NDC: 63629-1621
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: 63629-1621
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071457
Marketing Category: ANDA
Start Marketing Date: 19870421

Package Information of temazepam

Package NDC: 63629-1621-2
Package Description: 20 CAPSULE in 1 BOTTLE (63629-1621-2)

NDC Information of temazepam

NDC Code 63629-1621-2
Proprietary Name temazepam
Package Description 20 CAPSULE in 1 BOTTLE (63629-1621-2)
Product NDC 63629-1621
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 Bryant Ranch Prepack
Substance Name TEMAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of temazepam


General Information