prednisone
- Product NDC
- 70518-3555
- 11-digit product format
- 705183555
- Labeler code
- 70518
- Product ID
- 70518-3555_4f594705-dc5f-2448-e063-6394a90a222c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2022-10-17
- Substance
- PREDNISONE
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198148 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3555-0 | prednisone | 5 in 1 BOTTLE, PLASTIC | TABLET | 5 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3555 | PREDNISONE TABLET [REMEDYREPACK INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240327_b540f4af-8f07-4c56-b151-d759440c514a.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 |
|---|
| 70518-3555-0 | 70518355500 | 5 TABLET in 1 BOTTLE, PLASTIC (70518-3555-0) | 5 tablet | 2022-10-17 | 0000-00-00 | No | No | Current |