Dexamethasone
- Product NDC
- 63629-7850
- 11-digit product format
- 636297850
- Labeler code
- 63629
- Product ID
- 63629-7850_4a25abaa-862a-43f7-a3cc-4cfb056e6743
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA088306
- Marketing category
- ANDA
- Marketing start
- 1983-09-15
- 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 |
|---|
| 63629-7850-1 | 63629785001 | 30 TABLET in 1 BOTTLE (63629-7850-1) | 30 tablet | 1983-09-15 | No | No | Historical |
| 63629-7850-2 | 63629785002 | 1 TABLET in 1 BOTTLE (63629-7850-2) | 1 tablet | 1983-09-15 | No | No | Historical |
| 63629-7850-3 | 63629785003 | 100 TABLET in 1 BOTTLE (63629-7850-3) | 100 tablet | 2018-12-14 | No | No | Historical |