prednisone
- Product NDC
- 50090-7235
- 11-digit product format
- 500907235
- Labeler code
- 50090
- Product ID
- 50090-7235_58b1fd2b-906d-4807-92b1-560abe840fd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209727
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- Substance
- PREDNISONE
- Active strength
- 2.5 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 | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198146 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7235-0 | prednisone | 30 in 1 BOTTLE | TABLET | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7235 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 7 | Current NDC, 1 package rows | 20240830_d40a97f6-60d1-4dbc-b4dc-650d82af5fae.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 |
|---|
| 50090-7235-0 | 50090723500 | 30 TABLET in 1 BOTTLE (50090-7235-0) | 30 tablet | 2024-08-26 | No | No | Historical |