"68071-3420-7" National Drug Code (NDC)

Famotidine 14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-3420-7
Package Description14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)
Product NDC68071-3420
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220708
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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