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"51655-233-52" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-233-52
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)
Product NDC51655-233
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220817
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerNorthwind Pharmaceuticals, LLC
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/51655-233-52





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