HYDROCORTISONE
- Product NDC
- 71335-1989
- 11-digit product format
- 713351989
- Labeler code
- 71335
- Product ID
- 71335-1989_54e94095-73b5-4dfc-a0f7-1b97ea861f37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040646
- Marketing category
- ANDA
- Marketing start
- 2007-03-30
- Substance
- HYDROCORTISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WI4X0X7BPJ | HYDROCORTISONE | 50-23-7 | HYDROCORTISONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-1989-1 | 71335198901 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-1989-1) | 30 tablet | 2024-07-18 | No | No | Historical |
| 71335-1989-2 | 71335198902 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-1989-2) | 90 tablet | 2024-07-18 | No | No | Historical |
| 71335-1989-3 | 71335198903 | 58 TABLET in 1 BOTTLE, PLASTIC (71335-1989-3) | 58 tablet | 2024-07-18 | No | No | Historical |
| 71335-1989-4 | 71335198904 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-1989-4) | 28 tablet | 2024-07-18 | No | No | Historical |
| 71335-1989-5 | 71335198905 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-1989-5) | 60 tablet | 2021-11-11 | No | No | Historical |
| 71335-1989-6 | 71335198906 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-1989-6) | 100 tablet | 2024-07-18 | No | No | Historical |