"51079-746-19" National Drug Code (NDC)

Diltiazem Hydrochloride 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-746-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-746-17)
(Mylan Institutional Inc.)

NDC Code51079-746-19
Package Description25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-746-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-746-17)
Product NDC51079-746
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19960307
Marketing Category NameANDA
Application NumberANDA072838
ManufacturerMylan Institutional Inc.
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

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