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"68382-135-06" National Drug Code (NDC)

Losortan Potassium 30 TABLET, FILM COATED in 1 BOTTLE (68382-135-06)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-135-06
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68382-135-06)
Product NDC68382-135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosortan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101004
Marketing Category NameANDA
Application NumberANDA078243
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameLOSARTAN POTASSIUM
Strength25
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-135-06





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