NDC product
Buprenorphine 0.4mg/mL PF
NDC 26436-5500 · Hybrid Pharma
Key facts
| Product NDC | 26436-5500 |
|---|---|
| Proprietary name | Buprenorphine 0.4mg/mL PF |
| Nonproprietary name | Buprenorphine 0.4mg/mL PF |
| Substances | BUPRENORPHINE HYDROCHLORIDE |
| Dosage form | INJECTION |
| Route | INTRAMUSCULAR |
| Labeler | Hybrid Pharma |
| Product type | HUMAN COMPOUNDED DRUG |
| Marketing category | OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS) |
| DEA schedule | CIII |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory