Carvedilol
- Product NDC
- 0615-8018
- 11-digit product format
- 006158018
- Labeler code
- 0615
- Product ID
- 0615-8018_f97e1e8c-3ab2-489e-b1b5-7b5b479bfbd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA078332
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 2022-07-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0615-8018-30 | 00615801830 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8018-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2016-04-13 | 2022-07-31 | No | No | Current |
| 0615-8018-39 | 00615801839 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8018-39) | 2016-04-14 | 2022-07-31 | No | No | Current |