Register entry

Bausch & Lomb Incoporated

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Registered sites
0
Active NDC listings
2
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 human prescription drug. By marketing category: ANDA 2.

Dosage formNDCs
solution/ drops2
RouteNDCs
auricular (otic)1
ophthalmic1
Labeller name on the listingNDCs
bausch & lomb incoporated2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
Neomycin and Polymyxin B Sulfates and HydrocortisoneNeomycin Sulfate, Polymyxin B Sulfate, Hydrocortisonesolution/ drops, auricular (otic)24208-631ANDA
Sulfacetamide Sodium and Prednisolone Sodium PhosphateSulfacetamide Sodium and Prednisolone Sodium Phosphatesolution/ drops, ophthalmic24208-317ANDA
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Other companies listing neomycin sulfate, polymyxin b sulfate, hydrocortisone

Enquiry

Common questions

Is Bausch & Lomb Incoporated FDA approved?
Bausch & Lomb Incoporated holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Bausch & Lomb Incoporated make?
2 products are listed under Bausch & Lomb Incoporated in the openFDA NDC Directory, most often as solution/ drops. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.