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"68001-397-08" National Drug Code (NDC)

Famotidine 1000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)
(BluePoint Laboratories)

NDC Code68001-397-08
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)
Product NDC68001-397
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190619
Marketing Category NameANDA
Application NumberANDA206530
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/68001-397-08





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