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"63739-325-10" National Drug Code (NDC)

Famotidine 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-325-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(McKesson Corporation)

NDC Code63739-325-10
Package Description10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-325-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC63739-325
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075718
ManufacturerMcKesson Corporation
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/63739-325-10





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