"57664-117-13" National Drug Code (NDC)

Verapamil Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-117-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-117-13
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-117-13)
Product NDC57664-117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVerapamil Hydrochloride
Non-Proprietary NameVerapamil Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20120101
End Marketing Date20201130
Marketing Category NameANDA
Application NumberANDA090529
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameVERAPAMIL HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesP-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]

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