Prednisone
- Product NDC
- 50090-0096
- 11-digit product format
- 500900096
- Labeler code
- 50090
- Product ID
- 50090-0096_83cdad70-b6ad-4d3f-9071-87cefe966c3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA080292
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record