"68084-172-01" National Drug Code (NDC)

Famotidine 100 BLISTER PACK in 1 CARTON (68084-172-01) > 1 TABLET in 1 BLISTER PACK (68084-172-11)
(American Health Packaging)

NDC Code68084-172-01
Package Description100 BLISTER PACK in 1 CARTON (68084-172-01) > 1 TABLET in 1 BLISTER PACK (68084-172-11)
Product NDC68084-172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20070320
End Marketing Date20160131
Marketing Category NameANDA
Application NumberANDA090837
ManufacturerAmerican Health Packaging
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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