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"70518-2683-0" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2683-0)
(REMEDYREPACK INC.)

NDC Code70518-2683-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2683-0)
Product NDC70518-2683
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200408
Marketing Category NameANDA
Application NumberANDA074185
ManufacturerREMEDYREPACK INC.
Substance NameDILTIAZEM HYDROCHLORIDE
Strength120
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2683-0





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