prednisone
- Product NDC
- 68788-8212
- 11-digit product format
- 687888212
- Labeler code
- 68788
- Product ID
- 68788-8212_f9562b88-d50b-4a5a-9d39-b5bc33559313
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA213386
- Marketing category
- ANDA
- Marketing start
- 2022-06-07
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8212 | PREDNISONE TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240802_f9562b88-d50b-4a5a-9d39-b5bc33559313.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8212-1 | 68788821201 | 10 TABLET in 1 BOTTLE, PLASTIC (68788-8212-1) | 10 tablet | 2022-06-07 | 0000-00-00 | No | No | Current |
| 68788-8212-2 | 68788821202 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-8212-2) | 20 tablet | 2022-06-07 | 0000-00-00 | No | No | Current |
| 68788-8212-3 | 68788821203 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-8212-3) | 30 tablet | 2022-06-07 | 0000-00-00 | No | No | Current |
| 68788-8212-5 | 68788821205 | 15 TABLET in 1 BOTTLE, PLASTIC (68788-8212-5) | 15 tablet | 2022-06-07 | 0000-00-00 | No | No | Current |
| 68788-8212-8 | 68788821208 | 21 TABLET in 1 BOTTLE, PLASTIC (68788-8212-8) | 21 tablet | 2022-06-07 | 0000-00-00 | No | No | Current |