Fludrocortisone Acetate
- Product NDC
- 43063-714
- 11-digit product format
- 430630714
- Labeler code
- 43063
- Product ID
- 43063-714_7d39998d-0384-6e34-e053-2a91aa0a582b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludrocortisone Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040425
- Marketing category
- ANDA
- Marketing start
- 2003-02-14
- Marketing end
- 0000-00-00
- Substance
- FLUDROCORTISONE ACETATE
- Active strength
- 0 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record