Carvedilol
- Product NDC
- 63629-8039
- 11-digit product format
- 636298039
- Labeler code
- 63629
- Product ID
- 63629-8039_1b3d48e1-9ae6-46ad-989b-85bbc95942d7
- 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
- 2020-12-31
- 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 |
|---|
| 63629-8039-1 | 63629803901 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-8039-1) | 2019-07-18 | 0000-00-00 | No | No | Current |
| 63629-8039-2 | 63629803902 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-8039-2) | 2019-07-18 | 0000-00-00 | No | No | Current |