Carvedilol
- Product NDC
- 50090-1856
- 11-digit product format
- 500901856
- Labeler code
- 50090
- Product ID
- 50090-1856_93896706-1b3e-4c2b-8c97-affd6759d016
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078332
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 3 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1856-0 | 50090185600 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-1856-0) | 2015-06-02 | 0000-00-00 | No | No | Current |
| 50090-1856-1 | 50090185601 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-1856-1) | 2015-06-02 | 0000-00-00 | No | No | Current |
| 50090-1856-2 | 50090185602 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1856-2) | 2015-06-02 | 0000-00-00 | No | No | Current |
| 50090-1856-3 | 50090185603 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1856-3) | 2019-06-11 | 0000-00-00 | No | No | Current |