NDC 0409-2012 – Buprenorphine Hydrochloride
Buprenorphine Hydrochloride .3 mg/mL · Injection, Solution · Intramuscular, Intravenous
Product NDC0409-2012
Product details
- Brand name
- Buprenorphine Hydrochloride
- Generic name
- Buprenorphine Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous
- Marketing category
- ANDA · ANDA074137
- Marketed since
- June 14, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride .3 mg/mL
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0409-2012-32 | 10 CARTRIDGE in 1 CARTON (0409-2012-32) / 1 mL in 1 CARTRIDGE (0409-2012-03) | Jun 14, 2005 |
Recalls mentioning this NDC
- D-0564-2024 Jul 3, 2024 · Class II
Lack of Assurance of Sterility-The potential for incomplete crimp seals. - D-1604-2014 Oct 1, 2014 · Class II
Failed Impurities/Degradation Specification: Out of Specification results for pseudobuprenorphine impurity at the 9-month stability time point.
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