NDC 68071-3184 – Diclofenac Sodium Delayed Release
Diclofenac Sodium 50 mg/1 · Tablet, Delayed Release · Oral
Product NDC68071-3184
Product details
- Brand name
- Diclofenac Sodium Delayed Release
- Generic name
- Diclofenac Sodium
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075185
- Marketed since
- November 13, 1998
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diclofenac Sodium 50 mg/1
Uses, dosage, side effects and warnings for Diclofenac Sodium →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3184-1 | 21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-1) | Mar 21, 2017 |
| 68071-3184-2 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-2) | Mar 21, 2017 |
| 68071-3184-3 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-3) | Mar 21, 2017 |
| 68071-3184-5 | 45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-5) | Mar 21, 2017 |
| 68071-3184-6 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6) | Mar 21, 2017 |
| 68071-3184-9 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-9) | Mar 21, 2017 |
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