NDC 85509-1900 – Diclofenac Potassium
Diclofenac Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1900
Product details
- Brand name
- Diclofenac Potassium
- Generic name
- Diclofenac potassium
- Labeler
- PHOENIX RX LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215787
- Marketed since
- November 1, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diclofenac Potassium 50 mg/1
Uses, dosage, side effects and warnings for Diclofenac Potassium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1900-1 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-1900-1) | Jan 12, 2026 |
| 85509-1900-3 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-1900-3) | Nov 7, 2025 |
| 85509-1900-6 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-1900-6) | Jan 12, 2026 |
| 85509-1900-9 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-1900-9) | Jan 12, 2026 |
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