"0615-8301-39" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8301-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8301-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8301-39)
Product NDC0615-8301
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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