| Product NDC: | 63629-3979 |
| Proprietary Name: | Morphine Sulfate Extended Release |
| Non Proprietary Name: | Morphine Sulfate Extended Release |
| Active Ingredient(s): | 30 mg/1 & nbsp; Morphine Sulfate Extended Release |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63629-3979 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076412 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100318 |
| Package NDC: | 63629-3979-4 |
| Package Description: | 56 TABLET in 1 BOTTLE (63629-3979-4) |
| NDC Code | 63629-3979-4 |
| Proprietary Name | Morphine Sulfate Extended Release |
| Package Description | 56 TABLET in 1 BOTTLE (63629-3979-4) |
| Product NDC | 63629-3979 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine Sulfate Extended Release |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100318 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |