metoprolol succinate
- Product NDC
- 70518-2770
- 11-digit product format
- 705182770
- Labeler code
- 70518
- Product ID
- 70518-2770_d70bbafe-c058-5a22-e053-2995a90aea0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204161
- Marketing category
- ANDA
- Marketing start
- 2020-06-08
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| TH25PD4CCB | METOPROLOL SUCCINATE | 98418-47-4 | METOPROLOL SUCCINATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2770-0 | 70518277000 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2770-0) | 2020-06-08 | 0000-00-00 | No | No | Current |