Prednisone
- Product NDC
- 72189-489
- 11-digit product format
- 721890489
- Labeler code
- 72189
- Product ID
- 72189-489_2c4e30d6-25ee-5c75-e063-6294a90a2fc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2023-06-07
- Substance
- PREDNISONE
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198148 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-489-07 | Prednisone | 7 in 1 BOTTLE | TABLET | 7 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-489 | PREDNISONE TABLET [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_fd8eb82e-52df-c368-e053-6294a90ac6b0.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 |
|---|
| 72189-489-07 | 72189048907 | 7 TABLET in 1 BOTTLE (72189-489-07) | 7 tablet | 2023-06-07 | No | No | Current |