Prednisone
- Product NDC
- 70518-3537
- 11-digit product format
- 705183537
- Labeler code
- 70518
- Product ID
- 70518-3537_4f5700d9-f57c-3475-e063-6294a90a49df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 2023-09-27
- Substance
- PREDNISONE
- Active strength
- 5 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 | 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 |
|---|
| 70518-3537-0 | Prednisone | 1 in 1 CARTON | TABLET | 1 | | 7 |
| 70518-3537-0 | Prednisone | 21 in 1 BLISTER PACK | TABLET | 21 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3537 | PREDNISONE TABLET [REMEDYREPACK INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250501_4bd86b2f-75cb-4711-85e2-b81ed947cb13.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 |
|---|
| 70518-3537-0 | 70518353700 | 1 BLISTER PACK in 1 CARTON (70518-3537-0) / 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-09-27 | 0000-00-00 | No | No | Current |