"61919-455-60" National Drug Code (NDC)

Ranitidine 60 TABLET, FILM COATED in 1 BOTTLE (61919-455-60)
(DIRECT RX)

NDC Code61919-455-60
Package Description60 TABLET, FILM COATED in 1 BOTTLE (61919-455-60)
Product NDC61919-455
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerDIRECT RX
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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