Carvedilol
- Product NDC
- 63629-4070
- 11-digit product format
- 636294070
- Labeler code
- 63629
- Product ID
- 63629-4070_1a944182-f1d0-4294-9ecc-58dc18a80108
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077614
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 25 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4070-1 | 63629407001 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-4070-1) | 2009-06-02 | 0000-00-00 | No | No | Current |
| 63629-4070-2 | 63629407002 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4070-2) | 2009-06-02 | 0000-00-00 | No | No | Current |
| 63629-4070-3 | 63629407003 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4070-3) | 2009-06-02 | 0000-00-00 | No | No | Current |
| 63629-4070-4 | 63629407004 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4070-4) | 2009-06-02 | 0000-00-00 | No | No | Current |
| 63629-4070-5 | 63629407005 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4070-5) | 2009-06-02 | 0000-00-00 | No | No | Current |
| 63629-4070-6 | 63629407006 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4070-6) | 2009-09-10 | 0000-00-00 | No | No | Current |