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"72606-509-04" National Drug Code (NDC)

Famotidine 1000 TABLET, FILM COATED in 1 BOTTLE (72606-509-04)
(CELLTRION USA, INC.)

NDC Code72606-509-04
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (72606-509-04)
Product NDC72606-509
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200923
Marketing Category NameANDA
Application NumberANDA075786
ManufacturerCELLTRION 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/72606-509-04





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