| NDC Code | 82868-079-30 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-30) |
|---|
| Product NDC | 82868-079 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Metoprolol Succinate |
|---|
| Non-Proprietary Name | Metoprolol Succinate |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250606 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA216916 |
|---|
| Manufacturer | Northwind Health Company, LLC |
|---|
| Substance Name | METOPROLOL SUCCINATE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|