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Neomycin Polymyxin B Sulfates and Dexamethasone

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP (Sterile)

Approved
Approval ID

53c0710d-08e5-42ac-afb8-4faa13ae5833

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 19, 2012

Manufacturers
FDA

H.J. Harkins Company, Inc.

DUNS: 147681894

Products 1

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

Neomycin sulfate, Polymyxin B Sulfate and Dexamethasone

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code52959-085
Application NumberANDA064135
Product Classification
M
Marketing Category
C73584
G
Generic Name
Neomycin sulfate, Polymyxin B Sulfate and Dexamethasone
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateDecember 13, 2011
FDA Product Classification

INGREDIENTS (10)

Polymyxin B SulfateActive
Quantity: 10000 [USP'U] in 1 mL
Code: 19371312D4
Classification: ACTIM
DexamethasoneActive
Quantity: 1 mg in 1 mL
Code: 7S5I7G3JQL
Classification: ACTIB
BENZALKONIUM CHLORIDEInactive
Code: F5UM2KM3W7
Classification: IACT
Hydrochloric AcidInactive
Code: QTT17582CB
Classification: IACT
POLYSORBATE 20Inactive
Code: 7T1F30V5YH
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT
Sodium ChlorideInactive
Code: 451W47IQ8X
Classification: IACT
Neomycin SulfateActive
Quantity: 3.5 mg in 1 mL
Code: 057Y626693
Classification: ACTIM
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
Sodium HydroxideInactive
Code: 55X04QC32I
Classification: IACT

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Neomycin Polymyxin B Sulfates and Dexamethasone - FDA Drug Approval Details