Dapsone
- Product NDC
- 68151-2693
- 11-digit product format
- 681512693
- Labeler code
- 68151
- Product ID
- 68151-2693_793cbb6c-f958-4b97-b804-fe2817ab7142
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dapsone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA086841
- Marketing category
- ANDA
- Marketing start
- 2016-03-04
- Marketing end
- 0000-00-00
- Substance
- DAPSONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Sulfone [EPC],Sulfones [CS]
- 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 |
|---|
| 68151-2693-1 | Dapsone | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2693 | DAPSONE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20171228_13777ba5-17f0-4364-a754-af12514abbb0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2693-1 | 68151269301 | 1 in 1 BLISTER PACK | Historical |