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"70518-2132-0" National Drug Code (NDC)
Losartan Potassium 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2132-0)
(REMEDYREPACK INC.)
NDC Code
70518-2132-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2132-0)
Product NDC
70518-2132
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Losartan Potassium
Non-Proprietary Name
Losartan Potassium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190605
Marketing Category Name
ANDA
Application Number
ANDA090083
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/70518-2132-0