Metoprolol Succinate ER
- Product NDC
- 72189-652
- 11-digit product format
- 721890652
- Labeler code
- 72189
- Product ID
- 72189-652_45723206-1a9e-5299-e063-6294a90ad969
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate ER
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DIrect_Rx
- Application
- ANDA216916
- Marketing category
- ANDA
- Marketing start
- 2025-12-08
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 25 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoprolol Succinate ER
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL SUCCINATE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TH25PD4CCB |
| Rxcui | 866427 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-652-90 | Metoprolol Succinate ER | 90 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-652-90 | 72189065290 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-652-90) | 2025-12-08 | No | No | Current |