PREDNISONE
- Product NDC
- 68788-8858
- 11-digit product format
- 687888858
- Labeler code
- 68788
- Product ID
- 68788-8858_60bb6698-d1fc-4720-9954-266a3d650f0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA215672
- Marketing category
- ANDA
- Marketing start
- 2025-04-29
- 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 |
|---|
| 68788-8858-1 | PREDNISONE | 15 in 1 BOTTLE | TABLET | 15 | | 1 |
| 68788-8858-3 | PREDNISONE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8858 | PREDNISONE TABLET [PREFERRED PHARMACEUTICALS INC.] | 1 | Current NDC, 2 package rows | 20250430_60bb6698-d1fc-4720-9954-266a3d650f0d.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 |
|---|
| 68788-8858-1 | 68788885801 | 15 TABLET in 1 BOTTLE (68788-8858-1) | 15 tablet | 2025-04-29 | No | No | Historical |
| 68788-8858-3 | 68788885803 | 30 TABLET in 1 BOTTLE (68788-8858-3) | 30 tablet | 2025-04-29 | No | No | Historical |