"67046-172-20" National Drug Code (NDC)

Famotidine 20 TABLET, FILM COATED in 1 BLISTER PACK (67046-172-20)
(Contract Pharmacy Services-PA)

NDC Code67046-172-20
Package Description20 TABLET, FILM COATED in 1 BLISTER PACK (67046-172-20)
Product NDC67046-172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170920
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerContract Pharmacy Services-PA
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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