 
                        | Product NDC: | 0574-0153 | 
| Proprietary Name: | morphine sulfate | 
| Non Proprietary Name: | Morphine Suldate | 
| Active Ingredient(s): | 100 mg/5mL & nbsp; Morphine Suldate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0574-0153 | 
| Labeler Name: | Paddock Laboratories, LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA201574 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20120817 | 
| Package NDC: | 0574-0153-12 | 
| Package Description: | 1 BOTTLE in 1 CARTON (0574-0153-12) > 120 mL in 1 BOTTLE | 
| NDC Code | 0574-0153-12 | 
| Proprietary Name | morphine sulfate | 
| Package Description | 1 BOTTLE in 1 CARTON (0574-0153-12) > 120 mL in 1 BOTTLE | 
| Product NDC | 0574-0153 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Morphine Suldate | 
| Dosage Form Name | SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20120817 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Paddock Laboratories, LLC | 
| Substance Name | MORPHINE SULFATE | 
| Strength Number | 100 | 
| Strength Unit | mg/5mL | 
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |