DailyMed label
Buprenorphine Hydrochloride
DailyMed label · Hospira, Inc. · version 20
Key facts
| Product | Buprenorphine Hydrochloride |
|---|---|
| Labeler | Hospira, Inc. |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | BUPRENORPHINE HYDROCHLORIDE |
| Active ingredient UNIIs | 56W8MW3EN1 |
| Application number | 074137 |
| Route | INTRAMUSCULAR, INTRAVENOUS |
| DEA schedule | CIII |
| NDC package codes | 0409-2012-03, 0409-2012-32 |
| Effective date | Dec 31, 2025 |
| Set ID | 23aa1bb3-cecf-4e62-29bb-48488bb66fc3 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: