Dexamethasone
- Product NDC
- 70771-1704
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA216282
- Marketing category
- ANDA
- Substance
- DEXAMETHASONE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70771-1704-1 | 100 TABLET in 1 BOTTLE (70771-1704-1) | 2024-04-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dexamethasone Tablets | Zydus Lifesciences Limited | 2024-03-30 | HUMAN PRESCRIPTION DRUG LABEL | 2 |