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"68682-705-30" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-705-30)
(Oceanside Pharmaceuticals)

NDC Code68682-705-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-705-30)
Product NDC68682-705
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
ManufacturerOceanside Pharmaceuticals
Substance NameDILTIAZEM HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68682-705-30





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