temazepam - 54569-1726-1 - (temazepam)

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Drug Information of temazepam

Product NDC: 54569-1726
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: 54569-1726
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071457
Marketing Category: ANDA
Start Marketing Date: 19870421

Package Information of temazepam

Package NDC: 54569-1726-1
Package Description: 30 CAPSULE in 1 BOTTLE (54569-1726-1)

NDC Information of temazepam

NDC Code 54569-1726-1
Proprietary Name temazepam
Package Description 30 CAPSULE in 1 BOTTLE (54569-1726-1)
Product NDC 54569-1726
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 A-S Medication Solutions LLC
Substance Name TEMAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of temazepam


General Information