Diazepam - 49999-018-60 - (Diazepam)

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Drug Information of Diazepam

Product NDC: 49999-018
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: 49999-018
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071321
Marketing Category: ANDA
Start Marketing Date: 20111129

Package Information of Diazepam

Package NDC: 49999-018-60
Package Description: 60 TABLET in 1 BOTTLE (49999-018-60)

NDC Information of Diazepam

NDC Code 49999-018-60
Proprietary Name Diazepam
Package Description 60 TABLET in 1 BOTTLE (49999-018-60)
Product NDC 49999-018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111129
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information