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"68788-7665-3" National Drug Code (NDC)
Losartan Potassium 30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-7665-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)
Product NDC
68788-7665
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
20200228
Marketing Category Name
ANDA
Application Number
ANDA203835
Manufacturer
Preferred 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/68788-7665-3