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"72603-171-01" National Drug Code (NDC)

Famotidine 50 mL in 1 BOTTLE (72603-171-01)
(NorthStar Rx LLC)

NDC Code72603-171-01
Package Description50 mL in 1 BOTTLE (72603-171-01)
Product NDC72603-171
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20230907
Marketing Category NameANDA
Application NumberANDA215043
ManufacturerNorthStar Rx LLC
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/5mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72603-171-01





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