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"70786-0002-3" National Drug Code (NDC)

Famotidine 90 TABLET in 1 BOTTLE (70786-0002-3)
(Unit Dose Services)

NDC Code70786-0002-3
Package Description90 TABLET in 1 BOTTLE (70786-0002-3)
Product NDC70786-0002
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerUnit Dose Services
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70786-0002-3





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