"76162-031-56" National Drug Code (NDC)

Guaifenesin 4 BLISTER PACK in 1 CARTON (76162-031-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(TOPCO ASSOCIATES LLC)

NDC Code76162-031-56
Package Description4 BLISTER PACK in 1 CARTON (76162-031-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC76162-031
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20260422
Marketing Category NameANDA
Application NumberANDA210453
ManufacturerTOPCO ASSOCIATES LLC
Substance NameGUAIFENESIN
Strength1200
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

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