NDC 0143-9246
Buprenorphine Hydrochloride 0.324 mg per 1 mL injection
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.
Recalls
- Aug 14, 2020 · Class II · Hikma Pharmaceuticals USA Inc.
Sub-potent Drug: Out-of-Specification assay results found at 3 month stability testing.
Lots: Lot #s: 2005023.1, 2005024.1, 2005025.1, Exp 02/28/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 0.324 mg per 1 mL
- Approval
- ANDA ANDA076931
- On the market since
- May 25, 2005
- Package NDCs
0143-9246-010143-9246-05- Official label
- DailyMed (National Library of Medicine), updated Mar 13, 2025
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