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"61919-142-07" National Drug Code (NDC)

Loratadine 7 TABLET in 1 BOTTLE (61919-142-07)
(DirectRx)

NDC Code61919-142-07
Package Description7 TABLET in 1 BOTTLE (61919-142-07)
Product NDC61919-142
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20210913
End Marketing Date20231231
Marketing Category NameANDA
Application NumberANDA076301
ManufacturerDirectRx
Substance NameLORATADINE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-142-07





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