Carvedilol

Product NDC
68645-350
11-digit product format
686450350
Labeler code
68645
Product ID
68645-350_b4f2d5cd-dc9b-9d8c-e053-2995a90a02d2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Legacy Pharmaceutical Packaging, LLC
Application
ANDA077614
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68645-350-59EA - Each68645-3503c690a51-78b0-4673-8184-7adc9182f64c12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68645-350CARVEDILOL TABLET, FILM COATED [LEGACY PHARMACEUTICAL PACKAGING, LLC]13Legacy NDC20241012_0db9d532-d62c-46c5-b4b9-855d78d01314.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68645-350-596864503505960 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68645-350-59) 2007-09-050000-00-00NoNoCurrent