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"71679-309-00" National Drug Code (NDC)

Guaifenesin 38500 TABLET in 1 BOTTLE (71679-309-00)
(Health Pharma USA LLC)

NDC Code71679-309-00
Package Description38500 TABLET in 1 BOTTLE (71679-309-00)
Product NDC71679-309
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET
UsageORAL
Start Marketing Date20240207
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM012
ManufacturerHealth Pharma USA LLC
Substance NameGUAIFENESIN
Strength400
Strength Unitmg/1
Pharmacy ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71679-309-00





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