Sulindac
- Product NDC
- 68151-2871
- 11-digit product format
- 681512871
- Labeler code
- 68151
- Product ID
- 68151-2871_b3d696fb-eb14-4e42-acb8-1e897397aeda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulindac
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA071795
- Marketing category
- ANDA
- Marketing start
- 1990-04-03
- Marketing end
- 0000-00-00
- Substance
- SULINDAC
- Active strength
- 200 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2871-0 | Sulindac | 1 in 1 PACKAGE | TABLET | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2871 | SULINDAC TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140822_b8b549e9-53ec-407a-a505-b652faf8f3b6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2871-0 | 68151287100 | 1 in 1 PACKAGE | Historical |