Prednisone
- Product NDC
- 51407-922
- 11-digit product format
- 514070922
- Labeler code
- 51407
- Product ID
- 51407-922_2e6e74fa-2fa3-54bf-e063-6394a90abe04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 1985-12-04
- Substance
- PREDNISONE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 198145, 312615, 312617 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-922-10 | Prednisone | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-922 | PREDNISONE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 2 | Current NDC, 1 package rows | 20250221_1e05e071-0407-0970-e063-6294a90a6c65.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 |
|---|
| 51407-922-10 | 51407092210 | 1000 TABLET in 1 BOTTLE, PLASTIC (51407-922-10) | 1000 tablet | 2024-07-14 | No | No | Historical |