NDC 42023-179 – Buprenorphine Hydrochloride
Buprenorphine Hydrochloride .324 mg/mL · Injection · Intramuscular, Intravenous
Product NDC42023-179
Product details
- Brand name
- Buprenorphine Hydrochloride
- Generic name
- Buprenorphine Hydrochloride
- Labeler
- Par Health USA, LLC
- Dosage form
- Injection
- Route
- Intramuscular, Intravenous
- Marketing category
- ANDA · ANDA206586
- Marketed since
- July 30, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride .324 mg/mL
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42023-179-05 | 5 VIAL in 1 CARTON (42023-179-05) / 1 mL in 1 VIAL | Jul 30, 2015 |
Recalls mentioning this NDC
- D-0596-2026 Jun 24, 2026 · Class II
Crystallization; identified as Buprenorphine free base - D-0527-2026 May 20, 2026 · Class II
Crystallization; identified as Buprenorphine free base - D-0087-2024 Nov 15, 2023 · Class II
Crystallization; identified as Buprenorphine free base - D-0698-2017 May 17, 2017 · Class II
Crystallization: due to the presence of white, crystalline particulates, adhered to the side and bottom of the glass vials, which are comprised of principally dextrose and the buprenorphine active…
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