"0615-4582-39" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-4582-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-39)
Product NDC0615-4582
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100430
End Marketing Date20250831
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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