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"57664-757-99" National Drug Code (NDC)
Olmesartan Medoxomil 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-757-99)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-757-99
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-757-99)
Product NDC
57664-757
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
20161026
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA021286
Manufacturer
Sun Pharmaceutical Industries, 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/57664-757-99