NDC product
Buprenorphine Hydrochloride Sublingual
NDC 67046-997 · Contract Pharmacy Services-PA
Key facts
| Product NDC | 67046-997 |
|---|---|
| Proprietary name | Buprenorphine Hydrochloride Sublingual |
| Labeler | Contract Pharmacy Services-PA |
| Marketing category | ANDA |
| Application number | ANDA201066 |
| Marketing start | Mar 6, 2015 |
| Listing certified through | Dec 31, 2021 |
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 · Source date: