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"68180-725-06" National Drug Code (NDC)
Olmesartan Medoxomil 30 TABLET, FILM COATED in 1 BOTTLE (68180-725-06)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-725-06
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (68180-725-06)
Product NDC
68180-725
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
20170901
Marketing Category Name
ANDA
Application Number
ANDA206631
Manufacturer
Lupin Pharmaceuticals, Inc.
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/68180-725-06