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"68788-0999-3" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE (68788-0999-3)
(Preferred Pharmaceuticals, Inc)

NDC Code68788-0999-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-0999-3)
Product NDC68788-0999
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070905
Marketing Category NameANDA
Application NumberANDA076649
ManufacturerPreferred Pharmaceuticals, Inc
Substance NameCARVEDILOL
Strength3.125
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/68788-0999-3





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