buprenorphine hydrochloride is a Sublingual Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Buprenorphine Hydrochloride.
| Product ID | 63629-7125_047cf3bf-65d9-4d3e-aaaa-4f5c5c9364a2 |
| NDC | 63629-7125 |
| Product Type | Human Prescription Drug |
| Proprietary Name | buprenorphine hydrochloride |
| Generic Name | Buprenorphine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | SUBLINGUAL |
| Marketing Start Date | 2010-09-24 |
| Marketing Category | ANDA / |
| Application Number | ANDA090622 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
| Active Ingredient Strength | 2 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 |
| Marketing Start Date | 2016-10-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA090622 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-02-28 |
| Marketing End Date | 2018-02-28 |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0143-9246 | Buprenorphine Hydrochloride | Buprenorphine Hydrochloride |
| 0409-2012 | Buprenorphine Hydrochloride | Buprenorphine Hydrochloride |
| 0517-0725 | Buprenorphine Hydrochloride | Buprenorphine Hydrochloride |
| 21695-515 | Buprenorphine Hydrochloride | Buprenorphine Hydrochloride |
| 35356-556 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 42023-179 | Buprenorphine Hydrochloride | Buprenorphine Hydrochloride |
| 50090-1571 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 50383-924 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 50383-930 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 53217-246 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 70518-0442 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 63629-4092 | Buprenorphine hydrochloride | Buprenorphine hydrochloride |
| 63629-7126 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 64725-1924 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 64725-0930 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 67046-991 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 67046-990 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 70518-2216 | buprenorphine hydrochloride | buprenorphine hydrochloride |
| 55700-867 | BELBUCA | buprenorphine hydrochloride |
| 12496-0757 | Buprenex | buprenorphine hydrochloride |
| 50090-2924 | Buprenorphine | Buprenorphine Hydrochloride |
| 52440-100 | Probuphine | buprenorphine hydrochloride |