PredniSONE
- Product NDC
- 63629-6621
- 11-digit product format
- 636296621
- Labeler code
- 63629
- Product ID
- 63629-6621_00c7a5e2-742e-410b-827a-0cacf6e0d7cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA084122
- Marketing category
- ANDA
- Marketing start
- 2003-02-13
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record