Hydrocortisone
- Product NDC
- 0904-2674
- 11-digit product format
- 009042674
- Labeler code
- 0904
- Product ID
- 0904-2674_79c73b09-cff8-4376-9416-a581447f00c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA083365
- Marketing category
- ANDA
- Marketing start
- 1973-06-18
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record