HYDROCORTISONE
- Product NDC
- 54505-332
- 11-digit product format
- 545050332
- Labeler code
- 54505
- Product ID
- 54505-332_cf7e1e9e-371d-4f56-b26e-ff7d78617578
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lineage Therapeutics Inc
- Application
- ANDA040646
- Marketing category
- ANDA
- Marketing start
- 2007-03-30
- Marketing end
- 2019-11-30
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record