NDC 63629-4108 – Diclofenac Potassium
Diclofenac Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-4108
Product details
- Brand name
- Diclofenac Potassium
- Generic name
- Diclofenac Potassium
- Labeler
- Bryant Ranch Prepack
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 63629-4108-1 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-4108-1) | Dec 2, 2009 |
| 63629-4108-2 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4108-2) | Apr 20, 2010 |
| 63629-4108-3 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3) | May 25, 2010 |
| 63629-4108-4 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4108-4) | Jan 6, 2011 |
| 63629-4108-5 | 45 TABLET, FILM COATED in 1 BOTTLE (63629-4108-5) | Dec 22, 2021 |
| 63629-4108-6 | 58 TABLET, FILM COATED in 1 BOTTLE (63629-4108-6) | Dec 22, 2021 |
| 63629-4108-7 | 18 TABLET, FILM COATED in 1 BOTTLE (63629-4108-7) | Dec 22, 2021 |
| 63629-4108-8 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4108-8) | Dec 22, 2021 |
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