Prednisone
- Product NDC
- 60760-797
- 11-digit product format
- 607600797
- Labeler code
- 60760
- Product ID
- 60760-797_44723894-4127-bb7c-e063-6294a90a9c21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Substance
- PREDNISONE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 312615 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60760-797-12 | Prednisone | 12 in 1 BOTTLE, PLASTIC | TABLET | 12 | | 3 |
| 60760-797-21 | Prednisone | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-797 | PREDNISONE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 2 | Current NDC, 2 package rows | 20240824_1b3ea4cc-5bc6-ae47-e063-6294a90af13d.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 |
|---|
| 60760-797-12 | 60760079712 | 12 TABLET in 1 BOTTLE, PLASTIC (60760-797-12) | 12 tablet | 2024-08-19 | No | No | Current |
| 60760-797-21 | 60760079721 | 21 TABLET in 1 BOTTLE, PLASTIC (60760-797-21) | 21 tablet | 2024-06-19 | No | No | Current |