NDC product
QC Pink Bismuth
NDC 63868-171 · QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
Key facts
| Product NDC | 63868-171 |
|---|---|
| Proprietary name | QC Pink Bismuth |
| Nonproprietary name | Bismuth Subsalicylate |
| Substances | BISMUTH SUBSALICYLATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M008 |
| Marketing start | Apr 15, 2019 |
| Listing certified through | Dec 31, 2026 |
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: