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"0172-4357-70" National Drug Code (NDC)

Ranitidine 500 TABLET, FILM COATED in 1 BOTTLE (0172-4357-70)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0172-4357-70
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0172-4357-70)
Product NDC0172-4357
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19970912
Marketing Category NameANDA
Application NumberANDA075165
ManufacturerTeva Pharmaceuticals USA, Inc.
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/0172-4357-70





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