desonide
- Product NDC
- 0168-0310
- 11-digit product format
- 001680310
- Labeler code
- 0168
- Product ID
- 0168-0310_807659ea-f276-43d6-a187-0fe0f82493e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA075860
- Marketing category
- ANDA
- Marketing start
- 2002-03-19
- Marketing end
- 0000-00-00
- Substance
- DESONIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0168-0310-02 | 00168031002 | 1 BOTTLE in 1 CARTON (0168-0310-02) > 59 mL in 1 BOTTLE | 1 bottle | 2002-03-19 | 0000-00-00 | No | No | Current |
| 0168-0310-04 | 00168031004 | 1 BOTTLE in 1 CARTON (0168-0310-04) > 118 mL in 1 BOTTLE | 1 bottle | 2002-03-19 | 0000-00-00 | No | No | Current |