Dexamethasone
- Product NDC
- 70518-4320
- 11-digit product format
- 705184320
- Labeler code
- 70518
- Product ID
- 70518-4320_402e606f-d63d-9455-e063-6394a90a5994
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA215604
- Marketing category
- ANDA
- Marketing start
- 2025-03-25
- Substance
- DEXAMETHASONE
- Active strength
- 4 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 | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7S5I7G3JQL |
| Rxcui | 197582 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4320-0 | Dexamethasone | 4 in 1 BOTTLE, PLASTIC | TABLET | 4 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4320 | DEXAMETHASONE TABLET [REMEDYREPACK INC.] | 1 | Current NDC, 1 package rows | 20250327_8c5375a7-7a0d-4af0-8b86-bc87698ac3d1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4320-0 | 70518432000 | 4 TABLET in 1 BOTTLE, PLASTIC (70518-4320-0) | 4 tablet | 2025-03-25 | No | No | Historical |