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Fluconazole

Fluconazole Tablets USP Rx only

Approved
Approval ID

fe0cc56d-c0b6-f859-e053-6294a90ad932

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jun 13, 2023

Manufacturers
FDA

Pharmasource Meds, LLC

DUNS: 118772692

Products 1

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

Fluconazole

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code82982-070
Application NumberANDA077731
Product Classification
M
Marketing Category
C73584
G
Generic Name
Fluconazole
Product Specifications
Route of AdministrationORAL
Effective DateJune 13, 2023
FDA Product Classification

INGREDIENTS (7)

ANHYDROUS DIBASIC CALCIUM PHOSPHATEInactive
Code: L11K75P92J
Classification: IACT
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
FLUCONAZOLEActive
Quantity: 150 mg in 1 1
Code: 8VZV102JFY
Classification: ACTIB

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Fluconazole - FDA Drug Approval Details