Metoprolol Succinate
- Product NDC
- 68071-3965
- 11-digit product format
- 680713965
- Labeler code
- 68071
- Product ID
- 68071-3965_4b1ce29b-201b-66c6-e063-6394a90a62cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA207206
- Marketing category
- ANDA
- Marketing start
- 2022-04-27
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 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 TARTRATE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866436 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3965-9 | Metoprolol Succinate | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 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 |
|---|
| 68071-3965-9 | 68071396509 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3965-9) | 2026-02-18 | No | No | Historical |