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"61919-455-30" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BOTTLE (61919-455-30)
(Direct_Rx)

NDC Code61919-455-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-455-30)
Product NDC61919-455
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190812
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerDirect_Rx
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
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/61919-455-30





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