"70518-0783-0" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET in 1 BLISTER PACK (70518-0783-0)
(REMEDYREPACK INC.)

NDC Code70518-0783-0
Package Description30 TABLET in 1 BLISTER PACK (70518-0783-0)
Product NDC70518-0783
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20171011
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA018602
ManufacturerREMEDYREPACK INC.
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

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