"80513-711-03" National Drug Code (NDC)

Loratadine 300 TABLET in 1 BOTTLE (80513-711-03)
(Advanced Rx LLC)

NDC Code80513-711-03
Package Description300 TABLET in 1 BOTTLE (80513-711-03)
Product NDC80513-711
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20200101
Marketing Category NameANDA
Application NumberANDA210722
ManufacturerAdvanced Rx LLC
Substance NameLORATADINE
Strength10
Strength Unitmg/1

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