Prednisone
- Product NDC
- 68071-2445
- 11-digit product format
- 680712445
- Labeler code
- 68071
- Product ID
- 68071-2445_c449494b-5de2-5989-e053-2a95a90a5491
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2445 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210609_c449494b-5de1-5989-e053-2a95a90a5491.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2445-1 | 68071244501 | 100 TABLET in 1 BOTTLE (68071-2445-1) | 100 tablet | 2021-06-08 | 0000-00-00 | No | No | Current |