Metoprolol Succinate
- Product NDC
- 24979-038
- 11-digit product format
- 249790038
- Labeler code
- 24979
- Product ID
- 24979-038_19721ece-1989-43be-b7d3-c5415b5fd8d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- TWi Pharmaceuticals, Inc.
- Application
- ANDA207206
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 24979-038-01 | 24979003801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-038-01) | 2019-10-01 | 0000-00-00 | No | No | Current |
| 24979-038-02 | 24979003802 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-038-02) | 2019-10-01 | 0000-00-00 | No | No | Current |
| 24979-038-03 | 24979003803 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-038-03) | 2019-10-01 | 0000-00-00 | No | No | Current |