Drug

Who makes neomycin sulfate, polymyxin b sulfate and dexamethasone?

9 companies list neomycin sulfate, polymyxin b sulfate and dexamethasone as a human prescription drug, including under the names Maxitrol. Forms: ointment; suspension; suspension/ drops. Routes: ophthalmic.

Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology

Companies listing neomycin sulfate, polymyxin b sulfate and dexamethasone

CompanyFormsApplicationNDCsRegistered sites
NuCare Pharmaceuticals,Inc.United Statesointment; suspension; suspension/ dropsANDAANDA062341, ANDA064063, ANDA06413531
Sandoz Industrial Products S.AAustriaointment; suspensionANDA, NDAANDA062341, NDA05006525
Bausch & Lomb Ireland LimitedUnited Statesointment; suspension/ dropsANDAANDA064063, ANDA06413524
International Medication Systems, Ltd.United Statesointment; suspension/ dropsANDAANDA064063, ANDA06413523
Preferred Pharmaceuticals Inc.United Statesointment; suspension/ dropsANDAANDA064063, ANDA06413521
Proficient Rx LPUnited Statesointment; suspension/ dropsANDAANDA064063, ANDA06413521
Novartis Pharmaceuticals CorporationSwitzerlandointmentNDANDA050065120
Nordic Pharma, Inc.United StatessuspensionNDA AUTHORIZED GENERICNDA05002311
Harrow Eye, LLCsuspensionNDANDA05002310
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Common questions

Who makes neomycin sulfate, polymyxin b sulfate and dexamethasone?
9 companies list neomycin sulfate, polymyxin b sulfate and dexamethasone as a human prescription drug in the openFDA NDC Directory, led by NuCare Pharmaceuticals,Inc., Sandoz Industrial Products S.A, Bausch & Lomb Ireland Limited, International Medication Systems, Ltd., Preferred Pharmaceuticals Inc.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
Is there a generic Maxitrol?
6 companies list neomycin sulfate, polymyxin b sulfate and dexamethasone under an abbreviated new drug application (ANDA), the application type used for generics, and 3 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.