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"68788-7213-5" National Drug Code (NDC)
Losartan Potassium 50 TABLET, FILM COATED in 1 BOTTLE (68788-7213-5)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7213-5
Package Description
50 TABLET, FILM COATED in 1 BOTTLE (68788-7213-5)
Product NDC
68788-7213
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
20180719
Marketing Category Name
ANDA
Application Number
ANDA090083
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
LOSARTAN POTASSIUM
Strength
25
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/68788-7213-5