Dexamethasone
- Product NDC
- 82804-132
- 11-digit product format
- 828040132
- Labeler code
- 82804
- Product ID
- 82804-132_45fd8030-dbe3-4da4-9d0a-6549cf4f7359
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA201270
- Marketing category
- ANDA
- Marketing start
- 2023-07-17
- Substance
- DEXAMETHASONE
- Active strength
- 1.5 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 82804-132-21 | 82804013221 | 21 TABLET in 1 BOTTLE (82804-132-21) | 21 tablet | 2024-07-24 | No | No | Historical |