desoximetasone
- Product NDC
- 68788-7695
- 11-digit product format
- 687887695
- Labeler code
- 68788
- Product ID
- 68788-7695_05bd372d-ef4f-4e1c-8c7c-bb25d6c1c963
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desoximetasone
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205206
- Marketing category
- ANDA
- Marketing start
- 2020-03-20
- Marketing end
- 0000-00-00
- Substance
- DESOXIMETASONE
- Active strength
- 3 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68788-7695-6 | 68788769506 | 1 TUBE in 1 CARTON (68788-7695-6) > 60 g in 1 TUBE | 1 tube | 2020-03-20 | 0000-00-00 | No | No | Current |