"71205-276-90" National Drug Code (NDC)

Famotidine 90 TABLET, FILM COATED in 1 BOTTLE (71205-276-90)
(Proficient Rx LP)

NDC Code71205-276-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71205-276-90)
Product NDC71205-276
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerProficient Rx LP
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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