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"72865-215-30" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30)
(XLCare Pharmaceuticals, Inc.)

NDC Code72865-215-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30)
Product NDC72865-215
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211015
Marketing Category NameANDA
Application NumberANDA215689
ManufacturerXLCare Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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