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"0781-1884-13" National Drug Code (NDC)

Ranitidine Hydrochloride 10 BLISTER PACK in 1 CARTON (0781-1884-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Sandoz Inc)

NDC Code0781-1884-13
Package Description10 BLISTER PACK in 1 CARTON (0781-1884-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
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/0781-1884-13





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