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NDC 69238-7033-05 Fludrocortisone Acetate 0.1 mg/1 Details
Fludrocortisone Acetate 0.1 mg/1
Fludrocortisone Acetate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is FLUDROCORTISONE ACETATE.
MedlinePlus Drug Summary
Fludrocortisone, a corticosteroid, is used to help control the amount of sodium and fluids in your body. It is used to treat Addison's disease and syndromes where excessive amounts of sodium are lost in the urine. It works by decreasing the amount of sodium that is lost (excreted) in your urine. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 69238-7033-05Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Fludrocortisone Acetate
Product Information
| NDC | 69238-7033 |
|---|---|
| Product ID | 69238-7033_e873ee22-d1ef-496a-864d-d4820c76ea17 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Fludrocortisone Acetate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | FLUDROCORTISONE ACETATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 0.1 |
| Active Ingredient Units | mg/1 |
| Substance Name | FLUDROCORTISONE ACETATE |
| Labeler Name | Amneal Pharmaceuticals NY LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040431 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69238-7033-05 (69238703305)
| NDC Package Code | 69238-7033-5 |
|---|---|
| Billing NDC | 69238703305 |
| Package | 500 TABLET in 1 BOTTLE (69238-7033-5) |
| Marketing Start Date | 2002-03-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |