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"76420-713-90" National Drug Code (NDC)

Famotidine 90 TABLET, FILM COATED in 1 BOTTLE (76420-713-90)
(Asclemed USA, Inc.)

NDC Code76420-713-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (76420-713-90)
Product NDC76420-713
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230823
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerAsclemed USA, Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/76420-713-90





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