"0615-4582-31" National Drug Code (NDC)

Famotidine 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-31)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-4582-31
Package Description31 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-31)
Product NDC0615-4582
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100430
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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