Carvedilol
- Product NDC
- 35356-512
- 11-digit product format
- 353560512
- Labeler code
- 35356
- Product ID
- 35356-512_9d953464-0b6f-40ae-a2e7-cf39eda6a4fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078251
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 6 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
- 2023-12-31
- 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 |
|---|
| 35356-512-18 | 35356051218 | 180 TABLET, FILM COATED in 1 BOTTLE (35356-512-18) | 2007-09-05 | 0000-00-00 | No | No | Current |
| 35356-512-30 | 35356051230 | 30 TABLET, FILM COATED in 1 BOTTLE (35356-512-30) | 2007-09-05 | 0000-00-00 | No | No | Current |
| 35356-512-60 | 35356051260 | 60 TABLET, FILM COATED in 1 BOTTLE (35356-512-60) | 2007-09-05 | 0000-00-00 | No | No | Current |
| 35356-512-90 | 35356051290 | 90 TABLET, FILM COATED in 1 BOTTLE (35356-512-90) | 2007-09-05 | 0000-00-00 | No | No | Current |