Metoprolol Succinate
- Product NDC
- 62207-131
- 11-digit product format
- 622070131
- Labeler code
- 62207
- Product ID
- 62207-131_327de2c2-8091-50cc-e063-6394a90a14d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Granules India Ltd
- Application
- ANDA216509
- Marketing category
- ANDA
- Marketing start
- 2024-08-16
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 62207-131-49 | 62207013149 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-49) | 2024-08-16 | No | No | Historical |
| 62207-131-54 | 62207013154 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-54) | 2024-08-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol Succinate | Granules India Ltd | 2025-04-11 | HUMAN PRESCRIPTION DRUG LABEL | 2 |