"0615-3549-31" National Drug Code (NDC)

Diltiazem Hydrochloride 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-3549-31)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-3549-31
Package Description31 TABLET, FILM COATED in 1 BLISTER PACK (0615-3549-31)
Product NDC0615-3549
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20121204
Marketing Category NameANDA
Application NumberANDA072838
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

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