Prednisone
- Product NDC
- 63629-7335
- 11-digit product format
- 636297335
- Labeler code
- 63629
- Product ID
- 63629-7335_04dfdc0c-94b1-4568-9c8f-c2ec905bc7b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040392
- Marketing category
- ANDA
- Marketing start
- 2003-02-12
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record