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"0781-1884-31" National Drug Code (NDC)

Ranitidine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (0781-1884-31)
(Sandoz Inc)

NDC Code0781-1884-31
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0781-1884-31)
Product NDC0781-1884
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine Hydrochloride
Non-Proprietary NameRanitidine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19970829
Marketing Category NameANDA
Application NumberANDA074467
ManufacturerSandoz Inc
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
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/0781-1884-31





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