CARVEDILOL
- Product NDC
- 70518-3524
- 11-digit product format
- 705183524
- Labeler code
- 70518
- Product ID
- 70518-3524_e907252d-8f2a-13e6-e053-2a95a90a0af0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARVEDILOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078165
- Marketing category
- ANDA
- Marketing start
- 2022-09-17
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3524 | CARVEDILOL TABLET, FILM COATED [REMEDYREPACK INC.] | 4 | Legacy NDC | 20241011_9a4d0cad-71e8-40a9-8628-4e166ea9ecb3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3524-0 | 70518352400 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3524-0) | 2022-09-17 | 0000-00-00 | No | No | Current |