"67296-1383-3" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (67296-1383-3)
(RedPharm Drug, Inc.)

NDC Code67296-1383-3
Package Description30 TABLET in 1 BOTTLE (67296-1383-3)
Product NDC67296-1383
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerRedPharm Drug, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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