"49349-025-16" National Drug Code (NDC)

Ranitidine Hydrochloride 50 TABLET in 1 VIAL (49349-025-16)
(REMEDYREPACK INC.)

NDC Code49349-025-16
Package Description50 TABLET in 1 VIAL (49349-025-16)
Product NDC49349-025
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine Hydrochloride
Non-Proprietary NameRanitidine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20120112
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]

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