Fludrocortisone Acetate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceutical Corp. The primary component is Fludrocortisone Acetate.
Product ID | 0143-1246_18cc54af-63ba-47f7-a805-66b2da1f522e |
NDC | 0143-1246 |
Product Type | Human Prescription Drug |
Proprietary Name | Fludrocortisone Acetate |
Generic Name | Fludrocortisone Acetate |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2011-07-22 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA091302 |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | FLUDROCORTISONE ACETATE |
Active Ingredient Strength | 0 mg/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2011-07-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Ingredient | Strength |
---|---|
FLUDROCORTISONE ACETATE | .1 mg/1 |
SPL SET ID: | 198278e7-9a6d-4a9a-bb47-3589f35939da |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0115-7033 | Fludrocortisone Acetate | FLUDROCORTISONE ACETATE |
0143-1246 | Fludrocortisone Acetate | Fludrocortisone Acetate |
0555-0997 | Fludrocortisone Acetate | Fludrocortisone Acetate |
0615-6562 | Fludrocortisone Acetate | FLUDROCORTISONE ACETATE |
42291-529 | FLUDROCORTISONE ACETATE | FLUDROCORTISONE ACETATE |
42291-764 | Fludrocortisone Acetate | FLUDROCORTISONE ACETATE |
43063-714 | Fludrocortisone Acetate | Fludrocortisone Acetate |
50268-330 | FLUDROCORTISONE ACETATE | FLUDROCORTISONE ACETATE |
55154-6645 | Fludrocortisone Acetate | Fludrocortisone Acetate |
63629-7780 | Fludrocortisone Acetate | Fludrocortisone Acetate |
63629-8806 | Fludrocortisone Acetate | Fludrocortisone Acetate |
68084-288 | Fludrocortisone Acetate | Fludrocortisone Acetate |
69238-7033 | Fludrocortisone Acetate | FLUDROCORTISONE ACETATE |
70954-252 | Fludrocortisone Acetate | Fludrocortisone Acetate |
71335-0976 | Fludrocortisone Acetate | FLUDROCORTISONE ACETATE |