Deflazacort
- Product NDC
- 73190-068
- 11-digit product format
- 731900068
- Labeler code
- 73190
- Product ID
- 73190-068_459b75af-2b59-2f1e-e063-6394a90a9ed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Deflazacort
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA219254
- Marketing category
- ANDA
- Marketing start
- 2025-12-10
- Substance
- DEFLAZACORT
- Active strength
- 6 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
- Deflazacort
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEFLAZACORT | 6 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | KR5YZ6AE4B |
| Rxcui | 153098, 153880, 1870954, 1870958 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73190-068-01 | Deflazacort | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 73190-068-01 | Deflazacort | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73190-068-01 | 73190006801 | 1 BOTTLE in 1 CARTON (73190-068-01) / 100 TABLET in 1 BOTTLE | 1 bottle | 2025-12-10 | No | No | Current |