"70934-017-30" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-017-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-30)
Product NDC70934-017
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181025
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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