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"70771-1059-5" National Drug Code (NDC)
Olmesartan Medoxomil 500 TABLET, FILM COATED in 1 BOTTLE (70771-1059-5)
(Zydus Lifesciences Limited)
NDC Code
70771-1059-5
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (70771-1059-5)
Product NDC
70771-1059
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
20170424
Marketing Category Name
ANDA
Application Number
ANDA205192
Manufacturer
Zydus Lifesciences Limited
Substance Name
OLMESARTAN MEDOXOMIL
Strength
5
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/70771-1059-5