PREDNISONE
- Product NDC
- 68788-8898
- 11-digit product format
- 687888898
- Labeler code
- 68788
- Product ID
- 68788-8898_28130e6d-7cda-459a-9f80-cacaa82d71d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA215672
- Marketing category
- ANDA
- Marketing start
- 2025-08-01
- 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 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8898-5 | 68788889805 | 5 TABLET in 1 BOTTLE (68788-8898-5) | 5 tablet | 2025-08-01 | No | No | Historical |