Prednisone
- Product NDC
- 70954-057
- 11-digit product format
- 709540057
- Labeler code
- 70954
- Product ID
- 70954-057_373a92c5-ce0a-4d94-a75c-496751230950
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Substance
- PREDNISONE
- Active strength
- 2.5 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
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PREDNISONE | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198145, 198146, 198148, 312615, 312617, 763179, 763181, 763183, 763185 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70954-057-10 | Prednisone | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70954-057 | PREDNISONE TABLET [ANI PHARMACEUTICALS, INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250109_f05eb734-07e7-491c-b2e9-aae340e03750.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 |
|---|
| 70954-057-10 | 70954005710 | 100 TABLET in 1 BOTTLE (70954-057-10) | 100 tablet | 2019-11-15 | 0000-00-00 | No | No | Current |