Dexamethasone
- Product NDC
- 70771-1706
- 11-digit product format
- 707711706
- Labeler code
- 70771
- Product ID
- 70771-1706_232c68af-fb83-4b93-9e16-9803c8e680c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA216284
- Marketing category
- ANDA
- Marketing start
- 2024-05-13
- Substance
- DEXAMETHASONE
- Active strength
- 1 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 |
|---|
| 70771-1706-1 | 70771170601 | 100 TABLET in 1 BOTTLE (70771-1706-1) | 100 tablet | 2024-05-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dexamethasone Tablets, USP | Zydus Lifesciences Limited | 2024-05-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |