Hydrocortisone
- Product NDC
- 60687-511
- 11-digit product format
- 606870511
- Labeler code
- 60687
- Product ID
- 60687-511_c131a1d4-6f51-753d-e053-2995a90a9434
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA207029
- Marketing category
- ANDA
- Marketing start
- 2020-06-17
- Marketing end
- 2022-06-30
- Substance
- HYDROCORTISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-511-01 | 60687051101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-511-01) > 1 TABLET in 1 BLISTER PACK (60687-511-11) | 100 blister pack | 2020-03-01 | 0000-00-00 | No | No | Current |