Prednisone
- Product NDC
- 50090-1002
- 11-digit product format
- 500901002
- Labeler code
- 50090
- Product ID
- 50090-1002_73287fe3-e0e4-48a3-8c4a-6f37e6db6dd7
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Prednisone
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PREDNISONE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198145, 198146, 312615, 312617, 763183 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-1002-0 | Prednisone | 48 in 1 BOX, UNIT-DOSE | TABLET | 48 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1002 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 16 | Current NDC, 1 package rows | 20240525_efe0c82b-9dd9-4729-b06f-06307867aca0.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 |
|---|
| 50090-1002-0 | 50090100200 | 48 TABLET in 1 BOX, UNIT-DOSE (50090-1002-0) | 48 tablet | 2014-11-28 | No | No | Current |