Diazepam - 68788-9937-3 - (diazepam)

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Drug Information of Diazepam

Product NDC: 68788-9937
Proprietary Name: Diazepam
Non Proprietary Name: diazepam
Active Ingredient(s): 5    mg/1 & nbsp;   diazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diazepam

Product NDC: 68788-9937
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077749
Marketing Category: ANDA
Start Marketing Date: 20120117

Package Information of Diazepam

Package NDC: 68788-9937-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-9937-3)

NDC Information of Diazepam

NDC Code 68788-9937-3
Proprietary Name Diazepam
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68788-9937-3)
Product NDC 68788-9937
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120117
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information