"0093-2748-92" National Drug Code (NDC)

Famotidine 5 BLISTER PACK in 1 CARTON (0093-2748-92) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-2748-92
Package Description5 BLISTER PACK in 1 CARTON (0093-2748-92) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0093-2748
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150108
End Marketing Date20211126
Marketing Category NameANDA
Application NumberANDA075512
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1

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