Dapsone
- Product NDC
- 69543-151
- 11-digit product format
- 695430151
- Labeler code
- 69543
- Product ID
- 69543-151_9babe9c3-4ed2-46eb-a633-4999c86f87cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dapsone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- ANDA204074
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Marketing end
- 2021-10-31
- Substance
- DAPSONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Sulfone [EPC],Sulfones [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69543-151-30 | 69543015130 | 30 TABLET in 1 BOTTLE (69543-151-30) | 30 tablet | 2016-06-01 | 2021-10-31 | No | No | Current |