Prednisone
- Product NDC
- 42708-114
- 11-digit product format
- 427080114
- Labeler code
- 42708
- Product ID
- 42708-114_459c7779-af18-4654-e063-6294a90a9a2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QPharma, Inc.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42708-114-21 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-114 | PREDNISONE TABLET [QPHARMA, INC.] | 8 | Current NDC, Legacy NDC, 1 package rows | 20241127_f4d5974a-444f-4ef0-84a9-803150ccdeac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42708-114-21 | 42708011421 | 21 TABLET in 1 BOTTLE (42708-114-21) | 21 tablet | 2018-04-20 | 0000-00-00 | Yes | No | Current |