Metoprolol Succinate
- Product NDC
- 60050-002
- 11-digit product format
- 600500002
- Labeler code
- 60050
- Product ID
- 60050-002_a2d8f185-a2c4-bc6f-e053-2995a90aeea9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Pharmadax Inc.
- Application
- ANDA203028
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Additional Listing Data#
- Finished product
- No
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL SUCCINATE | 50 mg/1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60050-002-01 | 60050000201 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60050-002-01) | 2020-05-01 | 0000-00-00 | No | No | Current |
| 60050-002-10 | 60050000210 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (60050-002-10) | 2020-05-01 | 0000-00-00 | No | No | Current |