Metoprolol succinate
- Product NDC
- 71335-3069
- 11-digit product format
- 713353069
- Labeler code
- 71335
- Product ID
- 71335-3069_84ceb815-abd5-4073-9509-2bbd61c34af8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078889
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoprolol succinate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL SUCCINATE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TH25PD4CCB |
| Rxcui | 866419 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-3069-1 | Metoprolol succinate | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 1 |
| 71335-3069-2 | Metoprolol succinate | 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 |
|---|
| 71335-3069-1 | 71335306901 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3069-1) | 2026-02-06 | No | No | Historical |
| 71335-3069-2 | 71335306902 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3069-2) | 2026-02-06 | No | No | Historical |