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"16571-501-30" National Drug Code (NDC)
Losartan Potassium 30 TABLET, FILM COATED in 1 BOTTLE (16571-501-30)
(Rising Pharmaceuticals, Inc)
NDC Code
16571-501-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (16571-501-30)
Product NDC
16571-501
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Losartan Potassium
Non-Proprietary Name
Losartan Potassium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140730
Marketing Category Name
ANDA
Application Number
ANDA091497
Manufacturer
Rising Pharmaceuticals, Inc
Substance Name
LOSARTAN POTASSIUM
Strength
50
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/16571-501-30