Diclofenac Sodium
- Product NDC
- 71205-494
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075185
- Marketing category
- ANDA
- Substance
- DICLOFENAC SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-494-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-30) | 2020-10-20 | | No | Historical |
| 71205-494-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-60) | 2020-10-20 | | No | Historical |
| 71205-494-90 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-90) | 2020-10-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diclofenac Sodium | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |