"0172-5728-60" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0172-5728-60
Package Description100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)
Product NDC0172-5728
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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