NDC 0904-7155
Buprenorphine HCl
Buprenorphine Hcl
Buprenorphine HCl is a Sublingual Tablet in the Human Prescription Drug category. It is labeled and distributed by Major Pharmaceuticals. The primary component is Buprenorphine Hydrochloride.
| Product ID | 0904-7155_18414e03-9dcb-4665-820e-c8d082834879 |
| NDC | 0904-7155 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Buprenorphine HCl |
| Generic Name | Buprenorphine Hcl |
| Dosage Form | Tablet |
| Route of Administration | SUBLINGUAL |
| Marketing Start Date | 2009-10-08 |
| Marketing Category | ANDA / |
| Application Number | ANDA078633 |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
| Active Ingredient Strength | 8 mg/1 |
| Pharm Classes | Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] |
| DEA Schedule | CIII |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |