desoximetasone
- Product NDC
- 68382-936
- 11-digit product format
- 683820936
- Labeler code
- 68382
- Product ID
- 68382-936_0958031c-7ba1-4120-af13-48dd8e1958b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desoximetasone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA205620
- Marketing category
- ANDA
- Marketing start
- 2019-02-12
- 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
- 2021-12-31
- 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 |
|---|
| 68382-936-01 | 68382093601 | 1 TUBE in 1 CARTON (68382-936-01) > 15 g in 1 TUBE | 1 tube | 2019-02-12 | 0000-00-00 | No | No | Current |
| 68382-936-02 | 68382093602 | 1 TUBE in 1 CARTON (68382-936-02) > 60 g in 1 TUBE | 1 tube | 2019-02-12 | 0000-00-00 | No | No | Current |
| 68382-936-03 | 68382093603 | 1 TUBE in 1 CARTON (68382-936-03) > 100 g in 1 TUBE | 1 tube | 2019-02-12 | 0000-00-00 | No | No | Current |