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"49348-183-47" National Drug Code (NDC)

Sunmark Loratadine D 2 BLISTER PACK in 1 CARTON (49348-183-47) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(McKesson)

NDC Code49348-183-47
Package Description2 BLISTER PACK in 1 CARTON (49348-183-47) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC49348-183
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Loratadine D
Non-Proprietary NameLoratadine, Pseudoephedrine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20120306
End Marketing Date20190831
Marketing Category NameANDA
Application NumberANDA076050
ManufacturerMcKesson
Substance NameLORATADINE; PSEUDOEPHEDRINE SULFATE
Strength5; 120
Strength Unitmg/1; mg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-183-47





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