"68071-2185-2" National Drug Code (NDC)

Ranitidine 20 TABLET, FILM COATED in 1 BOTTLE (68071-2185-2)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2185-2
Package Description20 TABLET, FILM COATED in 1 BOTTLE (68071-2185-2)
Product NDC68071-2185
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
Strength150
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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