Metoprolol Succinate
- Product NDC
- 70518-3545
- 11-digit product format
- 705183545
- Labeler code
- 70518
- Product ID
- 70518-3545_e9eaf557-d6b7-3752-e053-2a95a90a5907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203699
- Marketing category
- ANDA
- Marketing start
- 2022-09-30
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], 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 |
|---|
| 70518-3545 | METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 4 | Legacy NDC | 20240326_56fa7b11-e67a-45e1-be5f-2e81fa679947.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3545-0 | 70518354500 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3545-0) | 2022-09-30 | 0000-00-00 | No | No | Current |