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"68382-135-16" National Drug Code (NDC)
Losortan Potassium 90 TABLET, FILM COATED in 1 BOTTLE (68382-135-16)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-135-16
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (68382-135-16)
Product NDC
68382-135
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Losortan Potassium
Non-Proprietary Name
Losartan Potassium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20101004
Marketing Category Name
ANDA
Application Number
ANDA078243
Manufacturer
Zydus Pharmaceuticals USA 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/68382-135-16