NDC product
tabcin ACTIVE
NDC 69729-809 · OPMX LLC.
Key facts
| Product NDC | 69729-809 |
|---|---|
| Proprietary name | tabcin ACTIVE |
| Nonproprietary name | Acetaminophen, Dextromethorphan Hydrobromide |
| Substances | DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | OPMX LLC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
| Marketing start | Jan 30, 2026 |
| Listing certified through | Dec 31, 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 · Source date: