"70000-0580-1" National Drug Code (NDC)

Guaifenesin D 1 BLISTER PACK in 1 CARTON (70000-0580-1) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(CARDINAL HEALTH 110, LLC. DBA LEADER)

NDC Code70000-0580-1
Package Description1 BLISTER PACK in 1 CARTON (70000-0580-1) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC70000-0580
Product Type NameHUMAN OTC DRUG
Proprietary NameGuaifenesin D
Non-Proprietary NameGuaifenesin And Pseudoephedrine Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210506
Marketing Category NameANDA
Application NumberANDA212542
ManufacturerCARDINAL HEALTH 110, LLC. DBA LEADER
Substance NameGUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength600; 60
Strength Unitmg/1; mg/1
Pharmacy ClassesAdrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC]

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