NDC 71335-1545

Carvedilol

Carvedilol

Carvedilol is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Carvedilol.

Product ID71335-1545_7aefb864-0a5f-4daf-ac83-28b3513f669a
NDC71335-1545
Product TypeHuman Prescription Drug
Proprietary NameCarvedilol
Generic NameCarvedilol
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2007-09-05
Marketing CategoryANDA / ANDA
Application NumberANDA077614
Labeler NameBryant Ranch Prepack
Substance NameCARVEDILOL
Active Ingredient Strength13 mg/1
Pharm ClassesAdrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71335-1545-1

30 TABLET, FILM COATED in 1 BOTTLE (71335-1545-1)
Marketing Start Date2010-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1545-5 [71335154505]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

NDC 71335-1545-3 [71335154503]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

NDC 71335-1545-1 [71335154501]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

NDC 71335-1545-6 [71335154506]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

NDC 71335-1545-2 [71335154502]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

NDC 71335-1545-4 [71335154504]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077614
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-03-30

Drug Details

NDC Crossover Matching brand name "Carvedilol" or generic name "Carvedilol"

NDCBrand NameGeneric Name
0093-0051CarvedilolCarvedilol
0093-0135CarvedilolCarvedilol
0093-7295CarvedilolCarvedilol
0093-7296CarvedilolCarvedilol
0378-3631Carvedilolcarvedilol
0378-3632Carvedilolcarvedilol
0378-3633Carvedilolcarvedilol
0378-3634Carvedilolcarvedilol
0615-6583CarvedilolCarvedilol
0615-6584CarvedilolCarvedilol
0615-6585CarvedilolCarvedilol
0615-6586CarvedilolCarvedilol
0615-7944CarvedilolCarvedilol
68001-152CarvedilolCarvedilol
68001-153CarvedilolCarvedilol
68001-154CarvedilolCarvedilol
68001-151CarvedilolCarvedilol
68071-1962CarvedilolCarvedilol
68071-1901CarvedilolCarvedilol
68071-1954CarvedilolCarvedilol
68071-3078CarvedilolCarvedilol
68071-3026CarvedilolCarvedilol
68071-3138CarvedilolCarvedilol
68071-1935CarvedilolCarvedilol
68071-3151CarvedilolCarvedilol
68071-3269CarvedilolCarvedilol
68071-4470CarvedilolCarvedilol
68071-4495CarvedilolCarvedilol
68071-4816CarvedilolCarvedilol
68071-4600CarvedilolCarvedilol
68084-843CarvedilolCarvedilol
68084-854CarvedilolCarvedilol
68084-876CarvedilolCarvedilol
68084-865CarvedilolCarvedilol
68382-094CarvedilolCarvedilol
68382-095CarvedilolCarvedilol
68382-092CarvedilolCarvedilol
68382-093CarvedilolCarvedilol
68462-162CarvedilolCarvedilol
68462-164CarvedilolCarvedilol
68462-165CarvedilolCarvedilol
68462-163CarvedilolCarvedilol
68645-350CarvedilolCarvedilol
68645-496CarvedilolCarvedilol
68645-351CarvedilolCarvedilol
68788-0999CarvedilolCarvedilol
68788-0254CarvedilolCarvedilol
68788-6817CarvedilolCarvedilol
68788-0253CarvedilolCarvedilol
68788-6819CarvedilolCarvedilol
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