prednisone
- Product NDC
- 50090-7219
- 11-digit product format
- 500907219
- Labeler code
- 50090
- Product ID
- 50090-7219_28290a6c-6b79-478e-a71b-a243a0605d11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- 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 |
|---|
| 50090-7219-0 | prednisone | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
| 50090-7219-1 | prednisone | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7219 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 4 | Current NDC, 2 package rows | 20240816_90b8b43e-01f9-4503-91c4-2b3cbae91a83.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 |
|---|
| 50090-7219-0 | 50090721900 | 60 TABLET in 1 BOTTLE (50090-7219-0) | 60 tablet | 2024-08-13 | No | No | Current |
| 50090-7219-1 | 50090721901 | 20 TABLET in 1 BOTTLE (50090-7219-1) | 20 tablet | 2024-08-13 | No | No | Current |