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Eprosartan Mesylate - 0378-6628-91 - (eprosartan mesylate)

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Drug Information of Eprosartan Mesylate

Product NDC: 0378-6628
Proprietary Name: Eprosartan Mesylate
Non Proprietary Name: eprosartan mesylate
Active Ingredient(s): 400    mg/1 & nbsp;   eprosartan mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Eprosartan Mesylate

Product NDC: 0378-6628
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202012
Marketing Category: ANDA
Start Marketing Date: 20120307

Package Information of Eprosartan Mesylate

Package NDC: 0378-6628-91
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6628-91)

NDC Information of Eprosartan Mesylate

NDC Code 0378-6628-91
Proprietary Name Eprosartan Mesylate
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6628-91)
Product NDC 0378-6628
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name eprosartan mesylate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120307
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name EPROSARTAN MESYLATE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Eprosartan Mesylate


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