Carvedilol

Product NDC
68788-7883
11-digit product format
687887883
Labeler code
68788
Product ID
68788-7883_6fd221f3-f96f-499a-9e4f-386aab3e5057
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmacdeuticals Inc
Application
ANDA078384
Marketing category
ANDA
Marketing start
2021-03-26
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7883-1EA - Each68788-7883ca94f3cb-9582-4b91-a421-36a528fd0cd612021-06-02
68788-7883-3EA - Each68788-78832698dce1-bdf4-46e1-92f9-6fe3660b88c312021-06-02
68788-7883-6EA - Each68788-788347d7d77b-aaa7-4fcb-8e4d-c97dbdb8805512021-06-02
68788-7883-8EA - Each68788-7883ee5f2194-c28a-4772-be2c-66f39173651b12021-06-02
68788-7883-9EA - Each68788-7883bf104cc9-757b-47ec-bae2-da1e5659bccf12021-06-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7883-168788788301100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-1) 2021-03-260000-00-00NoNoCurrent
68788-7883-36878878830330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-3) 2021-03-260000-00-00NoNoCurrent
68788-7883-66878878830660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-6) 2021-03-260000-00-00NoNoCurrent
68788-7883-868788788308120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-8) 2021-03-260000-00-00NoNoCurrent
68788-7883-96878878830990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7883-9) 2021-03-260000-00-00NoNoCurrent