DEXAMETHASONE
- Product NDC
- 72162-2600
- 11-digit product format
- 721622600
- Labeler code
- 72162
- Product ID
- 72162-2600_5ea02dfb-2164-44a3-b106-dd3bdec8fa09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE
- Dosage form
- ELIXIR
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA084754
- Marketing category
- ANDA
- Marketing start
- 2025-11-14
- Substance
- DEXAMETHASONE
- Active strength
- .5 mg/5mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DEXAMETHASONE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXAMETHASONE | .5 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7S5I7G3JQL |
| Rxcui | 309686 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2600-2 | DEXAMETHASONE | 237 mL in 1 BOTTLE | ELIXIR | 237 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2600-2 | 72162260002 | 237 mL in 1 BOTTLE (72162-2600-2) | 237 ml | 2026-01-09 | No | No | Historical |