PREDNISONE
- Product NDC
- 72189-275
- 11-digit product format
- 721890275
- Labeler code
- 72189
- Product ID
- 72189-275_cc330c63-1bb0-210d-e053-2995a90a2545
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2021-09-17
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-275-21 | PREDNISONE | 21 in 1 BOTTLE | TABLET | 21 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-275 | PREDNISONE TABLET [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20210918_c69e83a3-5217-ab76-e053-2995a90ae7c0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-275-21 | 72189027521 | 21 TABLET in 1 BOTTLE (72189-275-21) | 21 tablet | 2021-09-17 | 0000-00-00 | No | No | Current |