Prednisone
- Product NDC
- 82804-223
- 11-digit product format
- 828040223
- Labeler code
- 82804
- Product ID
- 82804-223_08973b30-8576-4d31-aeef-934b72124e1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Substance
- PREDNISONE
- Active strength
- 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 312617 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-223-10 | Prednisone | 10 in 1 BOTTLE | TABLET | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82804-223 | PREDNISONE TABLET [PROFICIENT RX LP] | 1 | Current NDC, 1 package rows | 20250511_08973b30-8576-4d31-aeef-934b72124e1f.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 |
|---|
| 82804-223-10 | 82804022310 | 10 TABLET in 1 BOTTLE (82804-223-10) | 10 tablet | 2025-05-02 | No | No | Current |