NDC 60290-088 – Diclofenac Potassium
Diclofenac Potassium 25 mg/1 · Tablet, Film Coated · Oral
Product NDC60290-088
Product details
- Brand name
- Diclofenac Potassium
- Generic name
- Diclofenac Potassium Tablets
- Labeler
- Umedica Laboratories USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215750
- Marketed since
- May 12, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diclofenac Potassium 25 mg/1
Uses, dosage, side effects and warnings for Diclofenac Potassium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 60290-088-01 | 30 TABLET, FILM COATED in 1 BOTTLE (60290-088-01) | Sep 28, 2024 |
| 60290-088-02 | 100 TABLET, FILM COATED in 1 BOTTLE (60290-088-02) | Sep 28, 2024 |
| 60290-088-03 | 500 TABLET, FILM COATED in 1 BOTTLE (60290-088-03) | Sep 28, 2024 |
| 60290-088-04 | 1000 TABLET, FILM COATED in 1 BOTTLE (60290-088-04) | Sep 28, 2024 |
| 60290-088-05 | 60 TABLET, FILM COATED in 1 BOTTLE (60290-088-05) | Oct 30, 2025 |
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