PREDNISONE
- Product NDC
- 60760-840
- 11-digit product format
- 607600840
- Labeler code
- 60760
- Product ID
- 60760-840_51c91bf1-6f2d-c0ab-e063-6394a90a71b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA215672
- Marketing category
- ANDA
- Marketing start
- 2025-11-05
- Substance
- PREDNISONE
- Active strength
- 20 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 | 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 |
|---|
| 60760-840-12 | PREDNISONE | 12 in 1 BOTTLE, PLASTIC | TABLET | 12 | | 5 |
| 60760-840-21 | PREDNISONE | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-840-12 | 60760084012 | 12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12) | 12 tablet | 2025-11-05 | No | No | Historical |
| 60760-840-21 | 60760084021 | 21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21) | 21 tablet | 2025-12-29 | No | No | Historical |