Prednisone
- Product NDC
- 50090-7023
- 11-digit product format
- 500907023
- Labeler code
- 50090
- Product ID
- 50090-7023_b2a00abf-3a97-4539-ab8f-be055e5971a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- Substance
- PREDNISONE
- Active strength
- 10 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
- Prednisone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PREDNISONE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198145 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7023-0 | Prednisone | 1 in 1 BLISTER PACK | TABLET | 1 | | 28 |
| 50090-7023-0 | Prednisone | 100 in 1 CARTON | TABLET | 100 | | 28 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7023 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 28 | Current NDC, 2 package rows | 20240229_95cf05e5-1446-43f5-8447-c04877a74781.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 |
|---|
| 50090-7023-0 | 50090702300 | 100 BLISTER PACK in 1 CARTON (50090-7023-0) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2024-01-08 | No | No | Current |