"0615-8033-39" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8033-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8033-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8033-39)
Product NDC0615-8033
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19951222
Marketing Category NameANDA
Application NumberANDA074185
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

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