Dexamethasone
- Product NDC
- 68788-7142
- 11-digit product format
- 687887142
- Labeler code
- 68788
- Product ID
- 68788-7142_516b5c33-de8c-47a1-ac2d-0396fe9a9410
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA084612
- Marketing category
- ANDA
- Marketing start
- 2018-04-19
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-7142-1 | 68788714201 | 12 TABLET in 1 BOTTLE, PLASTIC (68788-7142-1) | 12 tablet | 2018-04-19 | 0000-00-00 | No | No | Current |
| 68788-7142-3 | 68788714203 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7142-3) | 30 tablet | 2018-04-19 | 0000-00-00 | No | No | Current |
| 68788-7142-5 | 68788714205 | 15 TABLET in 1 BOTTLE, PLASTIC (68788-7142-5) | 15 tablet | 2018-04-19 | 0000-00-00 | No | No | Current |
| 68788-7142-6 | 68788714206 | 6 TABLET in 1 BOTTLE, PLASTIC (68788-7142-6) | 6 tablet | 2022-04-22 | 0000-00-00 | No | No | Current |