PREDNISONE
- Product NDC
- 67296-0600
- 11-digit product format
- 672960600
- Labeler code
- 67296
- Product ID
- 67296-0600_e59e1b07-a2b8-4d9b-9536-1734234d78dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA040392
- Marketing category
- ANDA
- Marketing start
- 2003-02-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67296-0600-1 | PREDNISONE | 10 in 1 BOTTLE | TABLET | 10 | | 1 |
| 67296-0600-2 | PREDNISONE | 15 in 1 BOTTLE | TABLET | 15 | | 1 |
| 67296-0600-3 | PREDNISONE | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0600 | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 3 package rows | 20110623_a651e06c-6295-4ed2-8d67-334645f05b30.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0600-1 | 67296060001 | 10 in 1 BOTTLE | Historical |
| 67296-0600-2 | 67296060002 | 15 in 1 BOTTLE | Historical |
| 67296-0600-3 | 67296060003 | 20 in 1 BOTTLE | Historical |