metoprolol succinate
- Product NDC
- 71205-800
- 11-digit product format
- 712050800
- Labeler code
- 71205
- Product ID
- 71205-800_57e33bcf-b380-44bb-b96e-3a637af6233a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204161
- Marketing category
- ANDA
- Marketing start
- 2020-02-03
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 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 |
|---|
| 71205-800-30 | 71205080030 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-800-30) | 2023-05-18 | No | No | Historical |
| 71205-800-60 | 71205080060 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-800-60) | 2023-05-18 | No | No | Historical |
| 71205-800-90 | 71205080090 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-800-90) | 2023-05-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| metoprolol succinate | Proficient Rx LP | 2023-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |