"16571-822-03" National Drug Code (NDC)

Loratadine 30 TABLET in 1 BOTTLE (16571-822-03)
(Rising Pharmaceuticals, Inc)

NDC Code16571-822-03
Package Description30 TABLET in 1 BOTTLE (16571-822-03)
Product NDC16571-822
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20220310
Marketing Category NameANDA
Application NumberANDA214684
ManufacturerRising Pharmaceuticals, Inc
Substance NameLORATADINE
Strength10
Strength Unitmg/1

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