NDC 71205-866 – Diclofenac Sodium Misoprostol
Diclofenac Sodium 75 mg/1; Misoprostol 200 ug/1 · Tablet, Delayed Release · Oral
Product NDC71205-866
Product details
- Brand name
- Diclofenac Sodium Misoprostol
- Generic name
- Diclofenac Sodium and Misoprostol
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205143
- Marketed since
- July 15, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug; Prostaglandin E1 Analog
Active ingredients
- Diclofenac Sodium 75 mg/1
- Misoprostol 200 ug/1
Uses, dosage, side effects and warnings for Diclofenac Sodium/Misoprostol →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-866-00 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-00) | Mar 7, 2022 |
| 71205-866-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-30) | Mar 7, 2022 |
| 71205-866-55 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-55) | Mar 7, 2022 |
| 71205-866-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-60) | Mar 7, 2022 |
| 71205-866-64 | 240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-64) | Mar 7, 2022 |
| 71205-866-72 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-72) | Mar 7, 2022 |
| 71205-866-90 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-90) | Mar 7, 2022 |
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