Carvedilol
- Product NDC
- 51079-771
- 11-digit product format
- 510790771
- Labeler code
- 51079
- Product ID
- 51079-771_d3af12b4-8e76-2323-e053-2a95a90ac0e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA077316
- Marketing category
- ANDA
- Marketing start
- 2007-09-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-771-20 | 51079077120 | 100 BLISTER PACK in 1 CARTON (51079-771-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-771-01) | 100 blister pack | 2007-09-14 | 0000-00-00 | No | No | Current |