PREDNISONE
- Product NDC
- 61919-226
- 11-digit product format
- 619190226
- Labeler code
- 61919
- Product ID
- 61919-226_9cac41a7-08f6-191c-e053-2a95a90af44d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA084283
- Marketing category
- ANDA
- Marketing start
- 2017-10-30
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-226-07 | PREDNISONE | 7 in 1 BOTTLE | TABLET | 7 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-226 | PREDNISONE TABLET [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200122_5cc817b3-b034-041b-e053-2a91aa0a4a30.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 |
|---|
| 61919-226-07 | 61919022607 | 7 TABLET in 1 BOTTLE (61919-226-07) | 7 tablet | 2017-10-30 | 0000-00-00 | No | No | Current |