Metoprolol Succinate
- Product NDC
- 63629-8237
- 11-digit product format
- 636298237
- Labeler code
- 63629
- Product ID
- 63629-8237_120c64fd-4302-4694-995a-41b91c7a4ebd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204106
- Marketing category
- ANDA
- Marketing start
- 2018-02-06
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 63629-8237-1 | 63629823701 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8237-1) | 2019-08-28 | 0000-00-00 | No | No | Current |
| 63629-8237-2 | 63629823702 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8237-2) | 2021-12-23 | 0000-00-00 | No | No | Current |
| 63629-8237-3 | 63629823703 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8237-3) | 2021-12-23 | 0000-00-00 | No | No | Current |