"70010-162-34" National Drug Code (NDC)

Loratadine 300 TABLET in 1 BOTTLE (70010-162-34)
(Granules Pharmaceuticals Inc.)

NDC Code70010-162-34
Package Description300 TABLET in 1 BOTTLE (70010-162-34)
Product NDC70010-162
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20200101
Marketing Category NameANDA
Application NumberANDA210722
ManufacturerGranules Pharmaceuticals Inc.
Substance NameLORATADINE
Strength10
Strength Unitmg/1

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