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"51079-752-20" National Drug Code (NDC)

Losartan Potassium 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-752-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-752-01)
(UDL Laboratories, Inc.)

NDC Code51079-752-20
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-752-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-752-01)
Product NDC51079-752
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110812
Marketing Category NameANDA
Application NumberANDA091590
ManufacturerUDL Laboratories, Inc.
Substance NameLOSARTAN POTASSIUM
Strength100
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/51079-752-20





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