Prednisone
- Product NDC
- 70518-2061
- 11-digit product format
- 705182061
- Labeler code
- 70518
- Product ID
- 70518-2061_880170e4-d0ce-5e31-e053-2a95a90af1c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040392
- Marketing category
- ANDA
- Marketing start
- 2019-05-03
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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