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Fludrocortisone Acetate

Approved
Approval ID

bf927cd9-1891-4de4-b4be-743a26363a64

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 3, 2010

Manufacturers
FDA

Physicians Total Care, Inc.

DUNS: 194123980

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

fludrocortisone acetate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code54868-5446
Application NumberANDA040431
Product Classification
M
Marketing Category
C73584
G
Generic Name
fludrocortisone acetate
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 3, 2010
FDA Product Classification

INGREDIENTS (5)

LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
FLUDROCORTISONE ACETATEActive
Quantity: 0.1 mg in 1 1
Code: V47IF0PVH4
Classification: ACTIB
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT

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Fludrocortisone Acetate - FDA Drug Approval Details