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"69848-017-02" National Drug Code (NDC)

Guaifenesin 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)
(GRANULES USA, INC.)

NDC Code69848-017-02
Package Description20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)
Product NDC69848-017
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20211231
Marketing Category NameANDA
Application NumberANDA213420
ManufacturerGRANULES USA, INC.
Substance NameGUAIFENESIN
Strength600
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/69848-017-02





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