"49349-025-03" National Drug Code (NDC)

Ranitidine Hydrochloride 20 TABLET in 1 BOTTLE (49349-025-03)
(REMEDYREPACK INC.)

NDC Code49349-025-03
Package Description20 TABLET in 1 BOTTLE (49349-025-03)
Product NDC49349-025
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine Hydrochloride
Non-Proprietary NameRanitidine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20131205
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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