PREDNISONE
- Product NDC
- 68071-5196
- 11-digit product format
- 680715196
- Labeler code
- 68071
- Product ID
- 68071-5196_d7732452-c96a-1a18-e053-2995a90a84a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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
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 |
|---|
| 68071-5196-1 | 68071519601 | 21 TABLET in 1 BOTTLE (68071-5196-1) | 21 tablet | 2020-03-10 | 0000-00-00 | No | No | Current |