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"63629-7669-7" National Drug Code (NDC)

Ranitidine 800 TABLET in 1 BOTTLE (63629-7669-7)
(Bryant Ranch Prepack)

NDC Code63629-7669-7
Package Description800 TABLET in 1 BOTTLE (63629-7669-7)
Product NDC63629-7669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20091216
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerBryant Ranch Prepack
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63629-7669-7





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