"64679-972-02" National Drug Code (NDC)

Famotidine 10 BLISTER PACK in 1 CARTON (64679-972-02) > 10 TABLET in 1 BLISTER PACK
(Wockhardt USA LLC.)

NDC Code64679-972-02
Package Description10 BLISTER PACK in 1 CARTON (64679-972-02) > 10 TABLET in 1 BLISTER PACK
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]

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