
USFDA APPLICATION NUMBER - 18704 / DOSAGE - INJECTABLE;INJECTION - 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| METOPROLOL TARTRATE(UNII: W5S57Y3A5L) (METOPROLOL - UNII:GEB06NHM23) | METOPROLOL TARTRATE | 5mg in 5 |
Inactive Ingredients
| Ingredient Name | Novartis Pharmaceuticals Corporation |
|---|---|
| SODIUM CHLORIDE(451W47IQ8X) | |
| WATER(059QF0KO0R) |