prednisone
- Product NDC
- 85766-086
- 11-digit product format
- 857660086
- Labeler code
- 85766
- Product ID
- 85766-086_503196db-b234-c296-e063-6394a90ae483
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sportpharm LLC
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2022-05-24
- Substance
- PREDNISONE
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198148 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85766-086-01 | 85766008601 | 100 TABLET in 1 BOTTLE (85766-086-01) | 100 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-05 | 85766008605 | 5 TABLET in 1 BOTTLE (85766-086-05) | 5 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-10 | 85766008610 | 10 TABLET in 1 BOTTLE (85766-086-10) | 10 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-20 | 85766008620 | 20 TABLET in 1 BOTTLE (85766-086-20) | 20 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-30 | 85766008630 | 30 TABLET in 1 BOTTLE (85766-086-30) | 30 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-60 | 85766008660 | 60 TABLET in 1 BOTTLE (85766-086-60) | 60 tablet | 2025-10-10 | No | No | Historical |
| 85766-086-90 | 85766008690 | 90 TABLET in 1 BOTTLE (85766-086-90) | 90 tablet | 2025-10-10 | No | No | Historical |