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 | 63629-7126_3e09672a-40d7-4e56-b625-15d488f711d7 |
NDC | 63629-7126 |
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 / ANDA |
Application Number | ANDA090622 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | BUPRENORPHINE HYDROCHLORIDE |
Active Ingredient Strength | 8 mg/1 |
Pharm Classes | Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC] |
DEA Schedule | CIII |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-11-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-04-26 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Marketing Category | ANDA |
Application Number | ANDA090622 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-11-01 |
Ingredient | Strength |
---|---|
BUPRENORPHINE HYDROCHLORIDE | 8 mg/1 |
SPL SET ID: | 8da7abe2-4f86-4d74-b819-57989f77a633 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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 |