"68071-3165-3" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BOTTLE (68071-3165-3)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-3165-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-3165-3)
Product NDC68071-3165
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20081119
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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