Hydrocortisone
- Product NDC
- 70518-1360
- 11-digit product format
- 705181360
- Labeler code
- 70518
- Product ID
- 70518-1360_92577d3a-2be6-0776-e053-2a95a90aa191
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085027
- Marketing category
- ANDA
- Marketing start
- 2018-08-09
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record