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"71205-212-30" National Drug Code (NDC)
Losartan Potassium 30 TABLET, FILM COATED in 1 BOTTLE (71205-212-30)
(Proficient Rx LP)
NDC Code
71205-212-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (71205-212-30)
Product NDC
71205-212
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
20101006
Marketing Category Name
ANDA
Application Number
ANDA090083
Manufacturer
Proficient Rx LP
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/71205-212-30