Carvedilol

Product NDC
58118-0163
11-digit product format
581180163
Labeler code
58118
Product ID
58118-0163_ae6b0b56-dda0-0dbf-e053-2a95a90a4063
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Clinical Solutions Wholesale
Application
ANDA078251
Marketing category
ANDA
Marketing start
2007-09-05
Marketing end
0000-00-00
Substance
CARVEDILOL
Active strength
6 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58118-0163CARVEDILOL TABLET, FILM COATED [CLINICAL SOLUTIONS WHOLESALE]10Legacy NDC20200904_5a5a9e29-1954-47a2-baa2-b34594130869.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
58118-0163-85811801630830 TABLET, FILM COATED in 1 BLISTER PACK (58118-0163-8) 2007-09-050000-00-00NoNoCurrent