FDA
Buprenorphine Hydrochloride
The FDA lists this product in 25 strengths and forms.
Composition
- Active ingredients
- BUPRENORPHINE HYDROCHLORIDE EQ 0.3MG BASE/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE · TabletANDA090279-002 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE · TabletANDA090279-001 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE · TabletANDA090819-001 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE · TabletANDA090819-002 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE · TabletANDA219401-001 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE · TabletANDA219401-002 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 0.3MG BASE/ML · InjectableANDA206586-001 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 0.3MG BASE/ML · InjectableThis page
- BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE · TabletANDA090622-001 · Prescription
- BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE · TabletANDA090622-002 · Prescription
At a glance
- Brand name
- Buprenorphine Hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- AM Regent
- Status
- Discontinued
- FDA approval
- 27 Mar 2007
- Application
- ANDA078331-001