| Product NDC: | 0527-1425 |
| Proprietary Name: | Morphine Sulfate |
| Non Proprietary Name: | Morphine Sulfate |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Morphine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0527-1425 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA201517 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110623 |
| Package NDC: | 0527-1425-35 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0527-1425-35) > 15 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 0527-1425-35 |
| Proprietary Name | Morphine Sulfate |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0527-1425-35) > 15 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0527-1425 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20110623 |
| Marketing Category Name | NDA |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |