"43602-501-30" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (43602-501-30)
(Ascent Pharmaceuticals, Inc.)

NDC Code43602-501-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (43602-501-30)
Product NDC43602-501
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211015
Marketing Category NameANDA
Application NumberANDA215689
ManufacturerAscent Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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