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"0093-0319-05" National Drug Code (NDC)

Diltiazem Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (0093-0319-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0319-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-0319-05)
Product NDC0093-0319
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19951222
Marketing Category NameANDA
Application NumberANDA074185
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0319-05





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