Morphine Sulfate Extended Release is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Morphine Sulfate.
| Product ID | 63629-3979_6302daf7-8b23-4633-ab2b-f7b7dc9f02b5 |
| NDC | 63629-3979 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Morphine Sulfate Extended Release |
| Generic Name | Morphine Sulfate Extended Release |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-03-18 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076412 |
| Labeler Name | bryant ranch prepack |
| Substance Name | MORPHINE SULFATE |
| Active Ingredient Strength | 30 mg/1 |
| Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule | CII |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2009-03-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA076412 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-03-18 |
| Inactivation Date | 2019-10-29 |
| Ingredient | Strength |
|---|---|
| MORPHINE SULFATE | 30 mg/1 |
| SPL SET ID: | fbfa1874-a710-49da-9e79-56cfaad69080 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 63629-3979 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 68084-157 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 68084-158 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 0904-6557 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 0904-6558 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 0904-6559 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 0904-6560 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 35356-833 | morphine sulfate extended release | morphine sulfate extended release |
| 35356-836 | morphine sulfate extended release | morphine sulfate extended release |
| 35356-838 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 42858-801 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 42858-802 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 42858-805 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 42858-804 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 42858-803 | Morphine Sulfate Extended Release | Morphine Sulfate Extended Release |
| 63629-4515 | morphine sulfate extended release | morphine sulfate extended release |
| 63629-4514 | morphine sulfate extended release | morphine sulfate extended release |