desoximetasone
- Product NDC
- 68382-889
- 11-digit product format
- 683820889
- Labeler code
- 68382
- Product ID
- 68382-889_4e8a68b7-f5a8-422b-a26a-04dc8f6e2d53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desoximetasone
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA205206
- Marketing category
- ANDA
- Marketing start
- 2017-12-05
- Marketing end
- 2022-07-31
- Substance
- DESOXIMETASONE
- Active strength
- 3 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- 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 |
|---|
| 68382-889-01 | 68382088901 | 1 TUBE in 1 CARTON (68382-889-01) > 15 g in 1 TUBE | 1 tube | 2017-12-05 | 2022-07-31 | No | No | Current |
| 68382-889-02 | 68382088902 | 1 TUBE in 1 CARTON (68382-889-02) > 60 g in 1 TUBE | 1 tube | 2017-12-05 | 2022-07-31 | No | No | Current |
| 68382-889-03 | 68382088903 | 1 TUBE in 1 CARTON (68382-889-03) > 100 g in 1 TUBE | 1 tube | 2017-12-05 | 2022-07-31 | No | No | Current |