"68788-7423-0" National Drug Code (NDC)

Ranitidine 14 TABLET in 1 BOTTLE (68788-7423-0)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7423-0
Package Description14 TABLET in 1 BOTTLE (68788-7423-0)
Product NDC68788-7423
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Proprietary Name SuffixImmediate Release
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160829
Marketing Category NameANDA
Application NumberANDA205512
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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