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"64679-972-03" National Drug Code (NDC)

Famotidine 40000 TABLET in 1 DRUM (64679-972-03)
(Wockhardt USA LLC.)

NDC Code64679-972-03
Package Description40000 TABLET in 1 DRUM (64679-972-03)
Product NDC64679-972
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20050307
Marketing Category NameANDA
Application NumberANDA077146
ManufacturerWockhardt USA LLC.
Substance NameFAMOTIDINE
Strength10
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/64679-972-03





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