| NDC Code | 63304-758-50 |
|---|
| Package Description | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50) |
|---|
| Product NDC | 63304-758 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Morphine Sulfate |
|---|
| Non-Proprietary Name | Morphine Sulfate |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120511 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078761 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | MORPHINE SULFATE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
|---|
| DEA Schedule | CII |
|---|