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"61919-391-32" National Drug Code (NDC)

Augmentin 5 mL in 1 BOTTLE (61919-391-32)
(Direct_Rx)

NDC Code61919-391-32
Package Description5 mL in 1 BOTTLE (61919-391-32)
Product NDC61919-391
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAugmentin
Non-Proprietary NameAmox/clav.pot.oral Susp
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20151109
Marketing Category NameANDA
Application NumberANDA065191
ManufacturerDirect_Rx
Substance NameAMOXICILLIN; CLAVULANIC ACID
Strength400; 57
Strength Unitmg/5mL; mg/5mL
Pharmacy ClassesPenicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-391-32





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