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"70518-0622-1" National Drug Code (NDC)

Ranitidine 90 TABLET in 1 BOTTLE, PLASTIC (70518-0622-1)
(REMEDYREPACK INC.)

NDC Code70518-0622-1
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-0622-1)
Product NDC70518-0622
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170717
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerREMEDYREPACK INC.
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/70518-0622-1





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