"66267-648-30" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (66267-648-30)
(NuCare Pharmaceuticals, Inc.)

NDC Code66267-648-30
Package Description30 TABLET in 1 BOTTLE (66267-648-30)
Product NDC66267-648
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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