Dexamethasone
- Product NDC
- 63629-4129
- 11-digit product format
- 636294129
- Labeler code
- 63629
- Product ID
- 63629-4129_4a25abaa-862a-43f7-a3cc-4cfb056e6743
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA084613
- Marketing category
- ANDA
- Marketing start
- 1975-06-03
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dexamethasone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXAMETHASONE | .75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7S5I7G3JQL |
| Rxcui | 197579, 197583, 343033 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4129-1 | 63629412901 | 12 TABLET in 1 BOTTLE (63629-4129-1) | 12 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |
| 63629-4129-2 | 63629412902 | 42 TABLET in 1 BOTTLE (63629-4129-2) | 42 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |
| 63629-4129-3 | 63629412903 | 30 TABLET in 1 BOTTLE (63629-4129-3) | 30 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |
| 63629-4129-4 | 63629412904 | 21 TABLET in 1 BOTTLE (63629-4129-4) | 21 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |
| 63629-4129-5 | 63629412905 | 20 TABLET in 1 BOTTLE (63629-4129-5) | 20 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |
| 63629-4129-6 | 63629412906 | 90 TABLET in 1 BOTTLE (63629-4129-6) | 90 tablet | 2010-02-08 | 0000-00-00 | No | No | Current |