METOPROLOL SUCCINATE
- Product NDC
- 49884-825
- 11-digit product format
- 498840825
- Labeler code
- 49884
- Product ID
- 49884-825_fcca559c-280e-4e44-b70c-6fe89ee3a277
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical Inc.
- Application
- NDA019962
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-11-21
- Marketing end
- 2021-05-31
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 49884-825-01 | 49884082501 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-825-01) | 2015-07-02 | 2021-05-31 | No | No | Current |
| 49884-825-10 | 49884082510 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-825-10) | 2015-08-11 | 2021-03-31 | No | No | Current |