Prednisone
- Product NDC
- 62135-470
- 11-digit product format
- 621350470
- Labeler code
- 62135
- Product ID
- 62135-470_45ae6dea-506e-55d8-e063-6394a90a0a4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA211496
- Marketing category
- ANDA
- Marketing start
- 2018-12-28
- Substance
- PREDNISONE
- Active strength
- 1 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 | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198144 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-470-18 | Prednisone | 180 in 1 BOTTLE | TABLET | 180 | | 2 |
| 62135-470-90 | Prednisone | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-470 | PREDNISONE TABLET [CHARTWELL RX, LLC] | 1 | Current NDC, 2 package rows | 20230125_f532c919-765d-407a-9e01-db2dc0c006f5.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 |
|---|
| 62135-470-18 | 62135047018 | 180 TABLET in 1 BOTTLE (62135-470-18) | 180 tablet | 2023-01-23 | No | No | Historical |
| 62135-470-90 | 62135047090 | 90 TABLET in 1 BOTTLE (62135-470-90) | 90 tablet | 2023-01-23 | No | No | Historical |