NDC 0517-0791
Betamethasone Sodium Phosphate and Betamethasone Acetate 3 mg per 1 mL injection, suspension
On the label: American Regent, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Hilliard, OH, United States | Makes it | Problems found, fixed voluntarilyJun 18, 2026 · 8 inspections |
| American Regent, Inc. | Columbus, OH, United States | Tests it | Problems found, fixed voluntarilyMar 5, 2026 · 8 inspections |
Product details
- Generic drug
- Betamethasone: every company that makes it
- Form
- injection, suspension, intra-articular; intralesional; intramuscular
- Strength
- 3 mg per 1 mL
- Approval
- ANDA ANDA090747
- On the market since
- Nov 1, 2019
- Package NDCs
0517-0791-01- Official label
- DailyMed (National Library of Medicine), updated Nov 19, 2025
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