Temazepam - 76237-250-39 - (Temazepam)

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Drug Information of Temazepam

Product NDC: 76237-250
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: 76237-250
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071427
Marketing Category: ANDA
Start Marketing Date: 20111206

Package Information of Temazepam

Package NDC: 76237-250-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (76237-250-39)

NDC Information of Temazepam

NDC Code 76237-250-39
Proprietary Name Temazepam
Package Description 30 CAPSULE in 1 BLISTER PACK (76237-250-39)
Product NDC 76237-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Temazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111206
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name TEMAZEPAM
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Temazepam


General Information