metoprolol succinate
- Product NDC
- 50090-5392
- 11-digit product format
- 500905392
- Labeler code
- 50090
- Product ID
- 50090-5392_930a2186-db9c-4bb0-ad02-786420a57772
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203894
- Marketing category
- ANDA
- Marketing start
- 2018-06-07
- 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
- 2021-12-31
- 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 |
|---|
| 50090-5392-0 | 50090539200 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5392-0) | 2020-11-24 | 0000-00-00 | No | No | Current |
| 50090-5392-1 | 50090539201 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5392-1) | 2020-11-24 | 0000-00-00 | No | No | Current |