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"70518-0801-3" National Drug Code (NDC)

Ranitidine 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0801-3)
(REMEDYREPACK INC.)

NDC Code70518-0801-3
Package Description28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0801-3)
Product NDC70518-0801
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171020
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/70518-0801-3





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