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"70518-1361-0" National Drug Code (NDC)

Ranitidine 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1361-0)
(REMEDYREPACK INC.)

NDC Code70518-1361-0
Package Description15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1361-0)
Product NDC70518-1361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180809
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerREMEDYREPACK INC.
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
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/70518-1361-0





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