Prednisone
- Product NDC
- 68071-3821
- 11-digit product format
- 680713821
- Labeler code
- 68071
- Product ID
- 68071-3821_31cfbc07-b041-ad9d-e063-6394a90ab204
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Substance
- PREDNISONE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198145 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3821-3 | Prednisone | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3821 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS, INC.] | 8 | Current NDC, 1 package rows | 20250410_31cfc21f-726b-ae80-e063-6294a90a9af4.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 |
|---|
| 68071-3821-3 | 68071382103 | 30 TABLET in 1 BOTTLE (68071-3821-3) | 30 tablet | 2025-04-02 | No | No | Historical |