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"72189-207-90" National Drug Code (NDC)

Famotidine 90 TABLET in 1 BOTTLE (72189-207-90)
(direct rx)

NDC Code72189-207-90
Package Description90 TABLET in 1 BOTTLE (72189-207-90)
Product NDC72189-207
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20210603
Marketing Category NameANDA
Application NumberANDA075805
Manufacturerdirect rx
Substance NameFAMOTIDINE
Strength40
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/72189-207-90





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