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"72162-1905-3" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1905-3)
(Bryant Ranch Prepack)

NDC Code72162-1905-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1905-3)
Product NDC72162-1905
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride Extended-release Tablets
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140206
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021392
ManufacturerBryant Ranch Prepack
Substance NameDILTIAZEM HYDROCHLORIDE
Strength360
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72162-1905-3





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