Metoprolol Succinate
- Product NDC
- 70934-542
- 11-digit product format
- 709340542
- Labeler code
- 70934
- Product ID
- 70934-542_aa6cb5ce-82ef-4fb9-e053-2995a90a99e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA207206
- Marketing category
- ANDA
- Marketing start
- 2020-02-06
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-542-30 | 70934054230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-542-30) | 2020-02-06 | 0000-00-00 | No | No | Current |
| 70934-542-90 | 70934054290 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-542-90) | 2020-04-07 | 0000-00-00 | No | No | Current |