Metoprolol succinate
- Product NDC
- 60760-993
- 11-digit product format
- 607600993
- Labeler code
- 60760
- Product ID
- 60760-993_4136fa6c-18b2-ccf4-e063-6294a90abda7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA213854
- Marketing category
- ANDA
- Marketing start
- 2025-02-01
- 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
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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TH25PD4CCB |
| Rxcui | 866436 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-993-90 | 60760099390 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-993-90) | 2025-10-15 | No | No | Historical |