Naltrexone is a Subcutaneous Implant in the Human Prescription Drug category. It is labeled and distributed by Complete Pharmacy And Medical Solutions. The primary component is Naltrexone; Triamcinolone.
| Product ID | 69364-3143_7b0350b5-ca48-4aef-8b10-ebd9f51967d0 |
| NDC | 69364-3143 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Naltrexone |
| Generic Name | Naltrexone |
| Dosage Form | Implant |
| Route of Administration | SUBCUTANEOUS |
| Marketing Start Date | 2018-02-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Complete Pharmacy and Medical Solutions |
| Substance Name | NALTREXONE; TRIAMCINOLONE |
| Active Ingredient Strength | 200 mg/1; mg/1 |
| Pharm Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2018-02-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2018-02-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| NALTREXONE | 200 mg/1 |
| SPL SET ID: | 40b16844-bc1c-485e-aad3-2cb86e2eb009 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 69364-3143 | Naltrexone | naltrexone |
| 65757-300 | VIVITROL | naltrexone |
| 65757-301 | VIVITROL | naltrexone |