Hydrocortisone
- Product NDC
- 43063-208
- 11-digit product format
- 430630208
- Labeler code
- 43063
- Product ID
- 43063-208_7f71eae7-6d5e-37ed-e053-2a91aa0ae7b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, In
- Application
- ANDA040761
- Marketing category
- ANDA
- Marketing start
- 2007-07-16
- Marketing end
- 2019-10-31
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record