Dexamethasone
- Product NDC
- 70771-1705
- 11-digit product format
- 707711705
- Labeler code
- 70771
- Product ID
- 70771-1705_ebc1bd42-82a5-40dc-ab21-b8d5252518b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA216282
- Marketing category
- ANDA
- Marketing start
- 2024-04-15
- Substance
- DEXAMETHASONE
- Active strength
- .75 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 |
|---|
| 70771-1705-1 | 70771170501 | 100 TABLET in 1 BOTTLE (70771-1705-1) | 100 tablet | 2024-04-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dexamethasone Tablets | Zydus Lifesciences Limited | 2024-03-30 | HUMAN PRESCRIPTION DRUG LABEL | 2 |