| 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] |