 
                        | Product NDC: | 0406-8003 | 
| Proprietary Name: | Morphine Sulfate | 
| Non Proprietary Name: | morphine sulfate | 
| Active Ingredient(s): | 20 mg/mL & nbsp; morphine sulfate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0406-8003 | 
| Labeler Name: | Mallinckrodt, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA202348 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20111003 | 
| Package NDC: | 0406-8003-15 | 
| Package Description: | 6 CARTON in 1 CASE (0406-8003-15) > 1 BOTTLE, PLASTIC in 1 CARTON > 15 mL in 1 BOTTLE, PLASTIC | 
| NDC Code | 0406-8003-15 | 
| Proprietary Name | Morphine Sulfate | 
| Package Description | 6 CARTON in 1 CASE (0406-8003-15) > 1 BOTTLE, PLASTIC in 1 CARTON > 15 mL in 1 BOTTLE, PLASTIC | 
| Product NDC | 0406-8003 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | morphine sulfate | 
| Dosage Form Name | SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20111003 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Mallinckrodt, Inc. | 
| Substance Name | MORPHINE SULFATE | 
| Strength Number | 20 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |