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"0093-0135-05" National Drug Code (NDC)

Carvedilol 500 TABLET, FILM COATED in 1 BOTTLE (0093-0135-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0135-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-0135-05)
Product NDC0093-0135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070906
Marketing Category NameANDA
Application NumberANDA076373
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameCARVEDILOL
Strength6.25
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0135-05





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