"64679-374-09" National Drug Code (NDC)

Famotidine 6500 TABLET in 1 DRUM (64679-374-09)
(Wockhardt USA LLC.)

NDC Code64679-374-09
Package Description6500 TABLET in 1 DRUM (64679-374-09)
Product NDC64679-374
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20100806
Marketing Category NameANDA
Application NumberANDA090837
ManufacturerWockhardt USA LLC.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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