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"51138-212-30" National Drug Code (NDC)
Benicar 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-212-30)
(Med-Health Pharma, LLC)
NDC Code
51138-212-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-212-30)
Product NDC
51138-212
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benicar
Non-Proprietary Name
Olmesartan Medoxomil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120202
Marketing Category Name
NDA
Application Number
NDA021286
Manufacturer
Med-Health Pharma, LLC
Substance Name
OLMESARTAN MEDOXOMIL
Strength
20
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/51138-212-30