Carvedilol

Product NDC
0904-6302
11-digit product format
009046302
Labeler code
0904
Product ID
0904-6302_c519a97b-5893-4a94-9923-1f867d08bdf1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA078227
Marketing category
ANDA
Marketing start
2012-11-14
Marketing end
0000-00-00
Substance
CARVEDILOL
Active strength
13 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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e148a93c-bfff-2735-e6c0-0739297b4596Product name320180705
32d6365f-9f0e-0782-b719-48e651893fb7Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6302-61EA - Each0904-63025e723a62-0a2f-4507-90b7-8e976181486712013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-6302CARVEDILOL TABLET, FILM COATED [MAJOR PHARMACEUTICALS]11Legacy NDC20241122_d5a28e57-7304-4e23-98a3-bae14d8ed25f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0904-6302-6100904630261100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6302-61) 2012-11-140000-00-00NoNoCurrent