Hydrocortisone
- Product NDC
- 50436-2144
- 11-digit product format
- 504362144
- Labeler code
- 50436
- Product ID
- 50436-2144_d1c3ba72-408f-4ef3-bd2d-c601dbedcfbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Unit Dose Services
- Application
- ANDA088799
- Marketing category
- ANDA
- Marketing start
- 2005-04-28
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 25 mg/g
- 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