 
                        | Product NDC: | 0409-6179 | 
| Proprietary Name: | Morphine Sulfate | 
| Non Proprietary Name: | MORPHINE SULFATE | 
| Active Ingredient(s): | 25 mg/mL & nbsp; MORPHINE SULFATE | 
| Administration Route(s): | INTRAVENOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0409-6179 | 
| Labeler Name: | Hospira, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 19910411 | 
| Package NDC: | 0409-6179-14 | 
| Package Description: | 1 VIAL in 1 CARTON (0409-6179-14) > 10 mL in 1 VIAL | 
| NDC Code | 0409-6179-14 | 
| Proprietary Name | Morphine Sulfate | 
| Package Description | 1 VIAL in 1 CARTON (0409-6179-14) > 10 mL in 1 VIAL | 
| Product NDC | 0409-6179 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | MORPHINE SULFATE | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 19910411 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Hospira, Inc. | 
| Substance Name | MORPHINE SULFATE | 
| Strength Number | 25 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |