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"51655-312-20" National Drug Code (NDC)

Famotidine 20 TABLET in 1 BOTTLE, PLASTIC (51655-312-20)
(Northwind Pharmaceuticals)

NDC Code51655-312-20
Package Description20 TABLET in 1 BOTTLE, PLASTIC (51655-312-20)
Product NDC51655-312
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20200521
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerNorthwind Pharmaceuticals
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/51655-312-20





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