Cortisone Acetate
- Product NDC
- 0143-9700
- 11-digit product format
- 001439700
- Labeler code
- 0143
- Product ID
- 0143-9700_5b33bc8b-1849-4469-a342-79324e3e643e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cortisone Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA080776
- Marketing category
- ANDA
- Marketing start
- 2013-08-22
- Marketing end
- 0000-00-00
- Substance
- CORTISONE ACETATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0143-9700-01 | 00143970001 | 100 TABLET in 1 BOTTLE (0143-9700-01) | 100 tablet | 2013-08-22 | 0000-00-00 | No | No | Current |