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"68001-240-08" National Drug Code (NDC)

Famotidine 1000 TABLET in 1 BOTTLE (68001-240-08)
(BluePoint Laboratories)

NDC Code68001-240-08
Package Description1000 TABLET in 1 BOTTLE (68001-240-08)
Product NDC68001-240
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerBluePoint Laboratories
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-240-08





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