NDC 0093-0948 – Diclofenac Potassium
Diclofenac Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-0948
Product details
- Brand name
- Diclofenac Potassium
- Generic name
- Diclofenac Potassium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075219
- Marketed since
- August 11, 1998
- Listing expires
- December 31, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-0948-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0948-01) | Aug 11, 1998 |
| 0093-0948-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-0948-05) | Aug 11, 1998 |
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