KLONOPIN - 16590-935-28 - (CLONAZEPAM)

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Drug Information of KLONOPIN

Product NDC: 16590-935
Proprietary Name: KLONOPIN
Non Proprietary Name: CLONAZEPAM
Active Ingredient(s): 1    mg/1 & nbsp;   CLONAZEPAM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of KLONOPIN

Product NDC: 16590-935
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017533
Marketing Category: NDA
Start Marketing Date: 19750602

Package Information of KLONOPIN

Package NDC: 16590-935-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (16590-935-28)

NDC Information of KLONOPIN

NDC Code 16590-935-28
Proprietary Name KLONOPIN
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (16590-935-28)
Product NDC 16590-935
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CLONAZEPAM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19750602
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name CLONAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of KLONOPIN


General Information