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"65084-645-41" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (65084-645-41)
(McKesson Corporation dba RX Pak)

NDC Code65084-645-41
Package Description30 TABLET in 1 BOTTLE (65084-645-41)
Product NDC65084-645
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
End Marketing Date20210430
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerMcKesson Corporation dba RX Pak
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/65084-645-41





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