NDC 0409-2012-32
Buprenorphine Hydrochloride .3 mg/mL
Buprenorphine Hydrochloride · INJECTION, SOLUTION
Buprenorphine Hydrochloride is a injection, solution containing buprenorphine hydrochloride at a strength of .3 mg/mL. Manufactured by Hospira, Inc..
Key Facts
- Brand Name
- Buprenorphine Hydrochloride
- Generic Name
- Buprenorphine Hydrochloride
- NDC Code (Package)
0409-2012-32- NDC Code (Product)
0409-2012- Manufacturer
- Hospira, Inc.
- Strength
- .3 mg/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Marketing Status
- DEA Schedule
- Schedule III (Controlled)
- Application #
- ANDA074137
- Marketing Start
- 06/14/2005
Recall History
No Recall HistoryView Full Drug Page
Buprenorphine Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.