METOPROLOL SUCCINATE
- Product NDC
- 49884-828
- 11-digit product format
- 498840828
- Labeler code
- 49884
- Product ID
- 49884-828_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
- 2007-07-26
- Marketing end
- 2021-04-30
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 200 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 |
|---|
| 49884-828-01 | 49884082801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-828-01) | 2015-07-02 | 2021-04-30 | No | No | Current |
| 49884-828-10 | 49884082810 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-828-10) | 2015-07-02 | 2021-04-30 | No | No | Current |