"51316-071-68" National Drug Code (NDC)

Guaifenesin 1 BLISTER PACK in 1 CARTON (51316-071-68) > 68 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(CVS)

NDC Code51316-071-68
Package Description1 BLISTER PACK in 1 CARTON (51316-071-68) > 68 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC51316-071
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20221007
Marketing Category NameANDA
Application NumberANDA209254
ManufacturerCVS
Substance NameGUAIFENESIN
Strength600
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

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