"42291-282-10" National Drug Code (NDC)

Famotidine 1000 TABLET in 1 BOTTLE (42291-282-10)
(AvKARE)

NDC Code42291-282-10
Package Description1000 TABLET in 1 BOTTLE (42291-282-10)
Product NDC42291-282
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20151116
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerAvKARE
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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