Carvedilol
- Product NDC
- 55154-6885
- 11-digit product format
- 551546885
- Labeler code
- 55154
- Product ID
- 55154-6885_79a44689-e948-4c79-af9a-94c5ebdcbbef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA078227
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-6885-0 | 55154688500 | 10 BLISTER PACK in 1 BAG (55154-6885-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2007-09-05 | 0000-00-00 | No | No | Current |