01 1ACETYLCHOLINE CHLORIDE
02 1ATROPINE SULFATE
03 1BEPOTASTINE BESILATE
04 1BESIFLOXACIN (BESIFLOXACIN HYDROCHLORIDE)
05 1BRIMONIDINE TARTRATE
06 1BROMFENAC (BROMFENAC SODIUM SESQUIHYDRATE)
07 1CLOFEDANOL HYDROCHLORIDE
08 1CYCLOPENTOLATE HYDROCHLORIDE
09 1FLUORESCEIN SODIUM
10 2GLYCERINE
11 1LATANOPROSTENE BUNOD
12 1LIFITEGRAST
13 4LOTEPREDNOL ETABONATE
14 2MINERAL OIL
15 1MINERAL OIL LIGHT
16 1NAPHAZOLINE HYDROCHLORIDE
17 1PERFLUOROHEXYLOCTANE
18 1PETROLATUM
19 1PHENIRAMINE MALEATE
20 2PHENYLEPHRINE HYDROCHLORIDE
21 1PILOCARPINE NITRATE
22 1PREDNISOLONE SODIUM PHOSPHATE
23 2PROPYLENE GLYCOL
24 2TETRACAINE HYDROCHLORIDE
25 1TROPICAMIDE
01 13DROPS
02 1GEL
03 3OINTMENT
04 1POWDER FOR SOLUTION
05 11SOLUTION
06 3SUSPENSION
07 1SYRUP
01 10.024%/W/V
02 10.025%/W/V
03 10.02675%/W/V
04 10.07%/W/V
05 10.2%/W/V
06 20.3%/W/V
07 10.315%/W/V
08 30.5%/W/V
09 20.5%/W/W
10 10.6%/W/V
11 11%
12 61%/W/V
13 11.5%/W/V
14 110%/W/V
15 1100%/W/W
16 22%/W/V
17 12.5%/W/V
18 120%
19 120MG/VIAL
20 125MG/5ML
21 14.5%
22 15%/W/V
23 180%
01 1ALREX
02 1BEPREVE
03 1BESIVANCE
04 1LOTEMAX
05 1LOTEMAX GEL
06 1LOTEMAX OINTMENT
07 2LUBRICANT EYE DROPS/ ARTIFICIAL TEARS
08 1LUMIFY
09 1MIEBO
10 1MINIMS ATROPINE SULPHATE
11 1MINIMS CYCLOPENTOLATE HYDROCHLORIDE
12 1MINIMS FLUORESCEIN SODIUM
13 2MINIMS PHENYLEPHRINE HYDROCHLORIDE
14 1MINIMS PILOCARPINE NITRATE
15 1MINIMS PREDNISOLONE SODIUM PHOSPHATE
16 2MINIMS TETRACAINE HYDROCHLORIDE
17 1MINIMS TROPICAMIDE
18 1MIOCHOL-E
19 1PROLENSA
20 2SOOTHE ALLERGY
21 2SOOTHE DRY EYES
22 2SOOTHE NIGHT TIME
23 2SOOTHE RESTORE
24 1ULONE
25 1VYZULTA
26 1XIIDRA
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 20MG/VIAL
Packaging : 2ML
Brand Name : MIOCHOL-E
Approval Date :
Application Number : 2133326
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 1%/W/V
Packaging : 20X0.3ML
Brand Name : MINIMS CYCLOPENTOLATE HYDROCH...
Approval Date :
Application Number : 2148382
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Ethical
Registration Country : Canada
Dosage Form : DROPS
Dosage Strength : 2%/W/V
Packaging : 0.3ML
Brand Name : MINIMS FLUORESCEIN SODIUM
Approval Date :
Application Number : 2148390
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : DROPS
Dosage Strength : 1%/W/V
Packaging : 20X0.3ML
Brand Name : MINIMS ATROPINE SULPHATE
Approval Date :
Application Number : 2148358
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SYRUP
Dosage Strength : 25MG/5ML
Packaging :
Brand Name : ULONE
Approval Date :
Application Number : 1966294
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 0.3%/W/V
Packaging : 3ML/15ML
Brand Name : SOOTHE DRY EYES
Approval Date :
Application Number : 2242370
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
BESIFLOXACIN (BESIFLOXACIN HYDROCHLORIDE)
Dosage Form : SUSPENSION
Dosage Strength : 0.6%/W/V
Packaging : 2ML/5ML
Brand Name : BESIVANCE
Approval Date :
Application Number : 2336847
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 1.5%/W/V
Packaging : 1/5/10ML
Brand Name : BEPREVE
Approval Date :
Application Number : 2456532
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 0.025%/W/V
Packaging :
Brand Name : LUMIFY
Approval Date :
Application Number : 2517698
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
BROMFENAC (BROMFENAC SODIUM SESQUIHYDRATE)
Dosage Form : SOLUTION
Dosage Strength : 0.07%/W/V
Packaging : 1.6ML/3ML
Brand Name : PROLENSA
Approval Date :
Application Number : 2439123
Regulatory Info : Prescription
Registration Country : Canada
Bausch & Lomb Incorporated is a supplier offers 2 products (APIs, Excipients or Intermediates).
Find a price of MANUFACTURING SITE,FACILITIES,PERSONNEL AND GENERAL OPERATING PROCEDURES IN TAMPA,FLORIDA. bulk offered by Bausch & Lomb Incorporated
Find a price of MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES IN GREENVILLE, SOUTH CAROLINA. bulk offered by Bausch & Lomb Incorporated
