"10135-763-90" National Drug Code (NDC)

Loratadine Allergy Relief 90 TABLET in 1 BOTTLE (10135-763-90)
(Marlex Pharmaceuticals, Inc.)

NDC Code10135-763-90
Package Description90 TABLET in 1 BOTTLE (10135-763-90)
Product NDC10135-763
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine Allergy Relief
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20221001
Marketing Category NameANDA
Application NumberANDA076134
ManufacturerMarlex Pharmaceuticals, Inc.
Substance NameLORATADINE
Strength10
Strength Unitmg/1

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