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"52125-890-19" National Drug Code (NDC)
Losortan Potassium 90 TABLET, FILM COATED in 1 BOTTLE (52125-890-19)
(REMEDYREPACK INC.)
NDC Code
52125-890-19
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (52125-890-19)
Product NDC
52125-890
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Losortan Potassium
Non-Proprietary Name
Losartan Potassium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140401
End Marketing Date
20171216
Marketing Category Name
ANDA
Application Number
ANDA078243
Manufacturer
REMEDYREPACK INC.
Substance Name
LOSARTAN POTASSIUM
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-890-19