NDC product
Sodium Sulfacetamide and Sulfur
NDC 63629-9259 · Bryant Ranch Prepack
Key facts
| Product NDC | 63629-9259 |
|---|---|
| Proprietary name | Sodium Sulfacetamide and Sulfur |
| Nonproprietary name | SULFACETAMIDE SODIUM, SULFUR |
| Substances | SULFACETAMIDE SODIUM, SULFUR |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Bryant Ranch Prepack |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Sulfonamide Antibacterial [EPC], Sulfonamides [CS] |
| Marketing start | Nov 15, 2021 |
| 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: