Fludrocortisone Acetate
- Product NDC
- 71335-0976
- 11-digit product format
- 713350976
- Labeler code
- 71335
- Product ID
- 71335-0976_4d482eab-8e9f-43f8-ac71-9762001f5266
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUDROCORTISONE ACETATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040431
- Marketing category
- ANDA
- Marketing start
- 2002-03-18
- Marketing end
- 0000-00-00
- Substance
- FLUDROCORTISONE ACETATE
- Active strength
- 0 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-0976-1 | 71335097601 | 30 TABLET in 1 BOTTLE (71335-0976-1) | 30 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-0976-2 | 71335097602 | 60 TABLET in 1 BOTTLE (71335-0976-2) | 60 tablet | 2018-10-23 | 0000-00-00 | No | No | Current |