prednisone
- Product NDC
- 60219-1705
- 11-digit product format
- 602191705
- Labeler code
- 60219
- Product ID
- 60219-1705_abdf7308-9460-4e7f-a68a-2fe647e82602
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA213385
- Marketing category
- ANDA
- Marketing start
- 2021-08-04
- Substance
- PREDNISONE
- Active strength
- 1 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 | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198144, 312617 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60219-1705-1 | prednisone | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-1705 | PREDNISONE TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 13 | Current NDC, Legacy NDC, 1 package rows | 20240922_0740ef68-7641-432e-bd46-4710687fc9d7.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 |
|---|
| 60219-1705-1 | 60219170501 | 100 TABLET in 1 BOTTLE, PLASTIC (60219-1705-1) | 100 tablet | 2021-08-04 | 0000-00-00 | No | No | Current |