prednisone
- Product NDC
- 68071-2771
- 11-digit product format
- 680712771
- Labeler code
- 68071
- Product ID
- 68071-2771_e456fb69-a686-4fa8-e053-2a95a90ae984
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2771-1 | prednisone | 10 in 1 BOTTLE, PLASTIC | TABLET | 10 | | 2 |
| 68071-2771-6 | prednisone | 6 in 1 BOTTLE, PLASTIC | TABLET | 6 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2771 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC, 2 package rows | 20220722_e3db385b-0629-fb20-e053-2a95a90ae901.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 |
|---|
| 68071-2771-1 | 68071277101 | 10 TABLET in 1 BOTTLE, PLASTIC (68071-2771-1) | 10 tablet | 2022-07-15 | 0000-00-00 | No | No | Current |
| 68071-2771-6 | 68071277106 | 6 TABLET in 1 BOTTLE, PLASTIC (68071-2771-6) | 6 tablet | 2022-07-15 | 0000-00-00 | No | No | Current |