"69842-335-16" National Drug Code (NDC)

Guaifenesin 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-16)
(CVS PHARMACY, INC)

NDC Code69842-335-16
Package Description14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-16)
Product NDC69842-335
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210301
Marketing Category NameANDA
Application NumberANDA213420
ManufacturerCVS PHARMACY, INC
Substance NameGUAIFENESIN
Strength1200
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

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