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ISOXSUPRINE HYDROCHLORIDE - 51293-605-01 - (isoxsuprine hydrochloride)

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Drug Information of ISOXSUPRINE HYDROCHLORIDE

Product NDC: 51293-605
Proprietary Name: ISOXSUPRINE HYDROCHLORIDE
Non Proprietary Name: isoxsuprine hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   isoxsuprine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ISOXSUPRINE HYDROCHLORIDE

Product NDC: 51293-605
Labeler Name: ECI Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110823

Package Information of ISOXSUPRINE HYDROCHLORIDE

Package NDC: 51293-605-01
Package Description: 100 TABLET in 1 BOTTLE (51293-605-01)

NDC Information of ISOXSUPRINE HYDROCHLORIDE

NDC Code 51293-605-01
Proprietary Name ISOXSUPRINE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOTTLE (51293-605-01)
Product NDC 51293-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isoxsuprine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110823
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name ECI Pharmaceuticals LLC
Substance Name ISOXSUPRINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ISOXSUPRINE HYDROCHLORIDE


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