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"76420-712-01" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01)
(Asclemed USA, Inc.)

NDC Code76420-712-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01)
Product NDC76420-712
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220708
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerAsclemed USA, Inc.
Substance NameFAMOTIDINE
Strength20
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/76420-712-01





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