NDC product
Betamethasone Sodium Phosphate and Betamethasone Acetate
NDC 0517-0720 · American Regent, Inc.
Key facts
| Product NDC | 0517-0720 |
|---|---|
| Proprietary name | Betamethasone Sodium Phosphate and Betamethasone Acetate |
| Nonproprietary name | Betamethasone Sodium Phosphate and Betamethasone Acetate |
| Substances | BETAMETHASONE ACETATE, BETAMETHASONE SODIUM PHOSPHATE |
| Dosage form | INJECTION, SUSPENSION |
| Route | INTRA-ARTICULAR, INTRALESIONAL, INTRAMUSCULAR |
| Labeler | American Regent, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA090747 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Apr 28, 2010 |
| 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: