PredniSONE
- Product NDC
- 68071-4862
- 11-digit product format
- 680714862
- Labeler code
- 68071
- Product ID
- 68071-4862_bb904a9f-51e4-f778-e053-2a95a90af1cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080352
- Marketing category
- ANDA
- Marketing start
- 1972-04-21
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4862-2 | 68071486202 | 20 TABLET in 1 BOTTLE (68071-4862-2) | 20 tablet | 2019-04-23 | 0000-00-00 | No | No | Current |