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"21130-179-67" National Drug Code (NDC)

Guaifenesin 1 BLISTER PACK in 1 CARTON (21130-179-67) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Better Living Brands LLC)

NDC Code21130-179-67
Package Description1 BLISTER PACK in 1 CARTON (21130-179-67) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC21130-179
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin
Non-Proprietary NameGuaifenesin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220415
Marketing Category NameANDA
Application NumberANDA210453
ManufacturerBetter Living Brands LLC
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/21130-179-67





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