NDC product
Orphenadrine Citrate
NDC 0185-0022 · Sandoz Inc
Key facts
| Product NDC | 0185-0022 |
|---|---|
| Proprietary name | Orphenadrine Citrate |
| Nonproprietary name | Orphenadrine Citrate |
| Substances | ORPHENADRINE CITRATE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Sandoz Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA040327 |
| Pharmacologic classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
| Marketing start | Feb 15, 2000 |
| Marketing end | Mar 20, 2027 |
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