TOPROL
- Product NDC
- 0186-1090
- 11-digit product format
- 001861090
- Labeler code
- 0186
- Product ID
- 0186-1090_03b2ba2e-c4b7-449d-8e07-9c0e08171f66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- NDA019962
- Marketing category
- NDA
- Marketing start
- 1992-02-01
- Marketing end
- 2021-05-31
- 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
- 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 |
|---|
| 0186-1090-05 | 00186109005 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1090-05) | 1992-02-01 | 2021-05-31 | No | No | Current |
| 0186-1090-35 | 00186109035 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1090-35) | 2016-06-07 | 2021-04-30 | No | No | Current |