SULINDAC
- Product NDC
- 71335-0413
- 11-digit product format
- 713350413
- Labeler code
- 71335
- Product ID
- 71335-0413_6db52fd3-172f-47ab-8aa6-4f3d031c6b25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sulindac
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072051
- Marketing category
- ANDA
- Marketing start
- 2009-09-04
- Marketing end
- 0000-00-00
- Substance
- SULINDAC
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-0413 | SULINDAC TABLET [BRYANT RANCH PREPACK] | 4 | Legacy NDC, 5 package rows | 20220129_6db52fd3-172f-47ab-8aa6-4f3d031c6b25.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0413-1 | 71335041301 | 30 TABLET in 1 BOTTLE (71335-0413-1) | 30 tablet | 2009-09-04 | 0000-00-00 | No | No | Current |
| 71335-0413-2 | 71335041302 | 60 TABLET in 1 BOTTLE (71335-0413-2) | 60 tablet | 2009-09-04 | 0000-00-00 | No | No | Current |
| 71335-0413-3 | 71335041303 | 20 TABLET in 1 BOTTLE (71335-0413-3) | 20 tablet | 2009-09-04 | 0000-00-00 | No | No | Current |
| 71335-0413-4 | 71335041304 | 14 TABLET in 1 BOTTLE (71335-0413-4) | 14 tablet | 2009-09-04 | 0000-00-00 | No | No | Current |
| 71335-0413-5 | 71335041305 | 90 TABLET in 1 BOTTLE (71335-0413-5) | 90 tablet | 2009-09-04 | 0000-00-00 | No | No | Current |