METOPROLOL SUCCINATE
- Product NDC
- 50090-3808
- 11-digit product format
- 500903808
- Labeler code
- 50090
- Product ID
- 50090-3808_56abf4fb-4584-4720-9ae0-cba6044595be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA019962
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-3808-0 | 50090380800 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3808-0) | 2018-01-01 | 0000-00-00 | No | No | Current |
| 50090-3808-1 | 50090380801 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3808-1) | 2018-11-09 | 0000-00-00 | No | No | Current |