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USFDA APPLICATION NUMBER - 19916 / DOSAGE - INJECTABLE;INJECTION - 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| MORPHINE SULFATE(UNII: X3P646A2J0) (MORPHINE - UNII:76I7G6D29C) | MORPHINE SULFATE | 5mg in 1 | 1mg in 1 | 0.5mg in 1 |
Inactive Ingredients
| Ingredient Name | Hospira, Inc. | REMEDYREPACK INC. |
|---|---|---|
| ANHYDROUS CITRIC ACID(XF417D3PSL) | ||
| HYDROCHLORIC ACID(QTT17582CB) | ||
| SODIUM CHLORIDE(451W47IQ8X) | ||
| SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) | ||
| SODIUM HYDROXIDE(55X04QC32I) | ||
| WATER(059QF0KO0R) |
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