Dexamethasone
- Product NDC
- 68071-2321
- 11-digit product format
- 680712321
- Labeler code
- 68071
- Product ID
- 68071-2321_d58ebf68-038a-7433-e053-2995a90a2108
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA084612
- Marketing category
- ANDA
- Marketing start
- 1978-07-19
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7S5I7G3JQL | DEXAMETHASONE | 50-02-2 | DEXAMETHASONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2321-1 | 68071232101 | 10 TABLET in 1 BOTTLE, PLASTIC (68071-2321-1) | 10 tablet | 2020-12-31 | 0000-00-00 | No | No | Current |
| 68071-2321-5 | 68071232105 | 15 TABLET in 1 BOTTLE, PLASTIC (68071-2321-5) | 15 tablet | 2020-12-31 | 0000-00-00 | No | No | Current |