prednisone
- Product NDC
- 45865-884
- 11-digit product format
- 458650884
- Labeler code
- 45865
- Product ID
- 45865-884_13177b28-fa9d-9732-e063-6394a90ab442
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- Substance
- PREDNISONE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 312615 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-884-21 | prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-884 | PREDNISONE TABLET [MEDSOURCE PHARMACEUTICALS] | 1 | Current NDC, 1 package rows | 20240308_131780a0-31f3-6588-e063-6294a90a2f8e.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 |
|---|
| 45865-884-21 | 45865088421 | 21 TABLET in 1 BOTTLE (45865-884-21) | 21 tablet | 2023-03-24 | No | No | Current |