TOPROL
- Product NDC
- 0186-1092
- 11-digit product format
- 001861092
- Labeler code
- 0186
- Product ID
- 0186-1092_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
- 2021-07-31
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 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 |
|---|
| 0186-1092-05 | 00186109205 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1092-05) | 1992-02-01 | 2021-07-31 | No | No | Current |
| 0186-1092-30 | 00186109230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1092-30) | 2014-07-15 | 2021-02-28 | No | No | Current |
| 0186-1092-35 | 00186109235 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1092-35) | 2016-06-07 | 2021-06-30 | No | No | Current |