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"70518-2127-0" National Drug Code (NDC)
Olmesartan Medoxomil 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2127-0)
(REMEDYREPACK INC.)
NDC Code
70518-2127-0
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2127-0)
Product NDC
70518-2127
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Olmesartan Medoxomil
Non-Proprietary Name
Olmesartan Medoxomil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190603
Marketing Category Name
ANDA
Application Number
ANDA207662
Manufacturer
REMEDYREPACK INC.
Substance Name
OLMESARTAN MEDOXOMIL
Strength
40
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/70518-2127-0