desonide
- Product NDC
- 0168-0309
- 11-digit product format
- 001680309
- Labeler code
- 0168
- Product ID
- 0168-0309_928b257f-8a7f-45b1-a2f9-c1ba834cb465
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA075751
- Marketing category
- ANDA
- Marketing start
- 2001-03-12
- Marketing end
- 0000-00-00
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0168-0309-15 | 00168030915 | 1 TUBE in 1 CARTON (0168-0309-15) > 15 g in 1 TUBE | 1 tube | 2001-03-12 | 0000-00-00 | No | No | Current |
| 0168-0309-60 | 00168030960 | 1 TUBE in 1 CARTON (0168-0309-60) > 60 g in 1 TUBE | 1 tube | 2001-03-12 | 0000-00-00 | No | No | Current |