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"61919-236-30" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (61919-236-30)
(DIRECT RX)

NDC Code61919-236-30
Package Description30 TABLET in 1 BOTTLE (61919-236-30)
Product NDC61919-236
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20171030
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerDIRECT RX
Substance NameFAMOTIDINE
Strength40
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/61919-236-30





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