PredniSONE
- Product NDC
- 70518-1116
- 11-digit product format
- 705181116
- Labeler code
- 70518
- Product ID
- 70518-1116_906e5ca9-e8ec-03c2-e053-2995a90a5fdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA080352
- Marketing category
- ANDA
- Marketing start
- 2018-04-19
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record