Prednisone
- Product NDC
- 60687-925
- 11-digit product format
- 606870925
- Labeler code
- 60687
- Product ID
- 60687-925_471886db-9b2e-83ba-e063-6394a90a26e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2025-12-29
- 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 | 198145, 198148, 312615 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-925-01 | Prednisone | 100 in 1 CARTON | TABLET | 100 | | 4 |
| 60687-925-11 | Prednisone | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-925-01 | 60687092501 | 100 BLISTER PACK in 1 CARTON (60687-925-01) / 1 TABLET in 1 BLISTER PACK (60687-925-11) | 100 blister pack | 2025-12-29 | No | No | Historical |
| 60687-925-11 | 60687092511 | 1 in 1 BLISTER PACK | | | | | Historical |