TOPROL
- Product NDC
- 0186-1094
- 11-digit product format
- 001861094
- Labeler code
- 0186
- Product ID
- 0186-1094_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
- 2021-04-30
- 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 |
|---|
| 0186-1094-05 | 00186109405 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1094-05) | 1992-02-01 | 2021-04-30 | No | No | Current |
| 0186-1094-30 | 00186109430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1094-30) | 2014-07-15 | 2021-02-28 | No | No | Current |
| 0186-1094-35 | 00186109435 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1094-35) | 2016-06-07 | 2021-04-30 | No | No | Current |