"70934-559-30" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET in 1 BOTTLE, PLASTIC (70934-559-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-559-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70934-559-30)
Product NDC70934-559
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20200303
End Marketing Date20230531
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA018602
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]

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