"68788-9874-3" National Drug Code (NDC)

Ranitidine 30 TABLET in 1 BOTTLE (68788-9874-3)
(Preferred Pharmaceuticals, Inc)

NDC Code68788-9874-3
Package Description30 TABLET in 1 BOTTLE (68788-9874-3)
Product NDC68788-9874
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20120227
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerPreferred Pharmaceuticals, Inc
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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