Prednisone
- Product NDC
- 72162-2149
- 11-digit product format
- 721622149
- Labeler code
- 72162
- Product ID
- 72162-2149_da85fbbc-ab2f-4bad-b592-5c1c53ecca97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080292
- Marketing category
- ANDA
- Marketing start
- 2019-03-07
- Substance
- PREDNISONE
- Active strength
- 5 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 | 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 |
|---|
| 72162-2149-0 | Prednisone | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2149 | PREDNISONE TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, 1 package rows | 20240830_91167f27-6f36-4b89-a530-be26209e4301.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 |
|---|
| 72162-2149-0 | 72162214900 | 1000 TABLET in 1 BOTTLE, PLASTIC (72162-2149-0) | 1000 tablet | 2019-03-07 | No | No | Historical |