prednisone
- Product NDC
- 60687-903
- 11-digit product format
- 606870903
- Labeler code
- 60687
- Product ID
- 60687-903_47fbb1fc-e212-0d31-e063-6294a90af3d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2026-01-09
- Substance
- PREDNISONE
- Active strength
- 5 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 312617 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-903-01 | prednisone | 10 in 1 CARTON | TABLET | 10 | | 2 |
| 60687-903-11 | prednisone | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-903-01 | 60687090301 | 10 BLISTER PACK in 1 CARTON (60687-903-01) / 1 TABLET in 1 BLISTER PACK (60687-903-11) | 10 blister pack | 2026-01-09 | No | No | Historical |
| 60687-903-11 | 60687090311 | 1 in 1 BLISTER PACK | | | | | Historical |