Prednisone
- Product NDC
- 68071-4319
- 11-digit product format
- 680714319
- Labeler code
- 68071
- Product ID
- 68071-4319_bb7a3bf3-db4e-d648-e053-2a95a90a8a2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA085162
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4319-3 | 68071431903 | 30 TABLET in 1 BOTTLE (68071-4319-3) | 30 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |