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USFDA APPLICATION NUMBER - 20080 / DOSAGE - INJECTABLE;SUBCUTANEOUS - EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| SUMATRIPTAN SUCCINATE(UNII: J8BDZ68989) (SUMATRIPTAN - UNII:8R78F6L9VO) | SUMATRIPTAN | 6mg in 0.5 | 4mg in 0.5 | 4mg in 0.5 | 6mg in 0.5 | 6mg in 0.5 |
Inactive Ingredients
| Ingredient Name | Glaxo Operations UK Ltd | Prasco Laboratories | Sandoz Inc |
|---|---|---|---|
| SODIUM CHLORIDE(451W47IQ8X) | |||
| WATER(059QF0KO0R) |
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