SULINDAC
- Product NDC
- 71205-648
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SULINDAC
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA072711
- Marketing category
- ANDA
- Substance
- SULINDAC
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71205-648-30 | 30 TABLET in 1 BOTTLE (71205-648-30) | 2022-03-28 | No | Historical | |
| 71205-648-60 | 60 TABLET in 1 BOTTLE (71205-648-60) | 2022-03-28 | No | Historical | |
| 71205-648-90 | 90 TABLET in 1 BOTTLE (71205-648-90) | 2022-03-28 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Sulindac Tablets USP, 200 mg Rx only | Proficient Rx LP | 2022-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |