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Bausch & Lomb Incorporated
FDA Orange Book

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.

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Inke S.A: APIs manufacturing plant.

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Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.

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Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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Bausch & Lomb Incorporated

VISIT THE VIRTUAL BOOTH, Contact Details

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Review portfolio & marketing content
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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

DIGITAL CONTENT

Interview #SpeakPharma, Vlog #PharmaReel, Data Compilation #PharmaFlow, 188 News #PharmaBuzz

Interview #SpeakPharma
Vlog #PharmaReel
Data Compilation #PharmaFlow
188 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

2 All APIs, 2 USDMF

2 All APIs
2 USDMF

DEVELOPMENTS

116 Drugs in Development

116 Drugs in Development

FINISHED DOSAGE FORMULATIONS

490 FDF Dossiers, 322 FDA Orange Book, 101 Europe, 35 Canada, 30 South Africa, 2 Listed Dossiers

490 FDF Dossiers
322 FDA Orange Book
101 Europe
35 Canada
30 South Africa
2 Listed Dossiers

INSPECTIONS & REGISTRATIONS

30 FDA, 3 EDQM, 1 GDUFA

30 FDA
3 EDQM
1 GDUFA

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FILTER :

filter Active Ingredients Reset all filters

322 All

01 2ACETIC ACID, GLACIAL; ALUMINUM ACETATE

02 1ACETIC ACID, GLACIAL; HYDROCORTISONE

03 1ACETYLCHOLINE CHLORIDE

04 2ACYCLOVIR

05 1ACYCLOVIR; HYDROCORTISONE

06 1ADAPALENE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE

07 2ALBUTEROL SULFATE

08 2ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE

09 1ATROPINE SULFATE

10 1BACITRACIN

11 3BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

12 2BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

13 2BACITRACIN ZINC; POLYMYXIN B SULFATE

14 1BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM

15 4BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE

16 1BEPOTASTINE BESILATE

17 1BESIFLOXACIN HYDROCHLORIDE

18 3BETAMETHASONE VALERATE

19 1BEXAROTENE

20 3BRIMONIDINE TARTRATE

21 1BRINZOLAMIDE

22 3BROMFENAC SODIUM

23 3BUPROPION HYDROBROMIDE

24 2BUPROPION HYDROCHLORIDE

25 1CARBACHOL

26 1CARTEOLOL HYDROCHLORIDE

27 2CHLORAMPHENICOL

28 2CHLORDIAZEPOXIDE HYDROCHLORIDE

29 1CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

30 1CICLOPIROX

31 1CLINDAMYCIN PHOSPHATE

32 1CLINDAMYCIN PHOSPHATE; TRETINOIN

33 3CROMOLYN SODIUM

34 3CYCLOPENTOLATE HYDROCHLORIDE

35 1DESIRUDIN RECOMBINANT

36 1DESMOPRESSIN ACETATE

37 1DEXAMETHASONE

38 3DEXAMETHASONE SODIUM PHOSPHATE

39 2DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

40 4DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

41 1DEXAMETHASONE; TOBRAMYCIN

42 7DIAZEPAM

43 1DICLOFENAC SODIUM

44 2DIHYDROERGOTAMINE MESYLATE

45 21DILTIAZEM HYDROCHLORIDE

46 1DIPIVEFRIN HYDROCHLORIDE

47 1DORZOLAMIDE HYDROCHLORIDE

48 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

49 2DOXYCYCLINE HYCLATE

50 2EDETATE CALCIUM DISODIUM

51 1EFINACONAZOLE

52 4ENALAPRIL MALEATE

53 2ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE

54 6ERYTHROMYCIN

55 2ERYTHROMYCIN ETHYLSUCCINATE

56 1ETHACRYNATE SODIUM

57 2ETHACRYNIC ACID

58 2FAMOTIDINE

59 2FENOFIBRATE

60 2FLUCYTOSINE

61 1FLUNISOLIDE

62 6FLUOCINOLONE ACETONIDE

63 1FLUOCINONIDE

64 1FLURBIPROFEN SODIUM

65 2GANCICLOVIR

66 6GENTAMICIN SULFATE

67 2GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

68 2GRISEOFULVIN, ULTRAMICROSIZE

69 1HALOBETASOL PROPIONATE

70 1HALOBETASOL PROPIONATE; TAZAROTENE

71 2HYALURONIDASE

72 8HYDROCORTISONE

73 3HYDROCORTISONE BUTYRATE

74 6HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

75 1HYDROXYPROPYL CELLULOSE

76 4HYDROXYZINE HYDROCHLORIDE

77 3IMIQUIMOD

78 3IPRATROPIUM BROMIDE

79 1ISOPROTERENOL HYDROCHLORIDE

80 5ISOSORBIDE DINITRATE

81 3KANAMYCIN SULFATE

82 3KETOTIFEN FUMARATE

83 1LATANOPROST

84 1LATANOPROSTENE BUNOD

85 2LEVOBUNOLOL HYDROCHLORIDE

86 1LIFITEGRAST

87 3LORAZEPAM

88 5LOTEPREDNOL ETABONATE

89 1LOTEPREDNOL ETABONATE; TOBRAMYCIN

90 1LULICONAZOLE

91 2METHAZOLAMIDE

92 1METHOXSALEN

93 2METHYLTESTOSTERONE

94 1METIPRANOLOL HYDROCHLORIDE

95 2METRONIDAZOLE

96 1METYROSINE

97 12MINOCYCLINE HYDROCHLORIDE

98 1MINOXIDIL

99 1NABILONE

100 3NAPHAZOLINE HYDROCHLORIDE

101 1NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

102 1NITROGLYCERIN

103 1NYSTATIN

104 2NYSTATIN; TRIAMCINOLONE ACETONIDE

105 2OFLOXACIN

106 2OLOPATADINE HYDROCHLORIDE

107 1ORPHENADRINE CITRATE

108 1PEGAPTANIB SODIUM

109 1PENTOXIFYLLINE

110 1PERFLUOROHEXYLOCTANE

111 1PHENDIMETRAZINE TARTRATE

112 1PHYTONADIONE

113 1PIMECROLIMUS

114 2PIRBUTEROL ACETATE

115 1PODOFILOX

116 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

117 4PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

118 5PREDNISOLONE SODIUM PHOSPHATE

119 1PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

120 2PROCAINAMIDE HYDROCHLORIDE

121 2PROPARACAINE HYDROCHLORIDE

122 4PYRIDOSTIGMINE BROMIDE

123 1RIBAVIRIN

124 1SELEGILINE HYDROCHLORIDE

125 1SODIUM BENZOATE; SODIUM PHENYLACETATE

126 8SULFACETAMIDE SODIUM

127 1TAZAROTENE

128 2TETRABENAZINE

129 1TETRACAINE HYDROCHLORIDE

130 9TIMOLOL MALEATE

131 1TOBRAMYCIN

132 2TOLCAPONE

133 6TRETINOIN

134 4TRIAMCINOLONE ACETONIDE

135 1TRIENTINE HYDROCHLORIDE

136 4TROPICAMIDE

137 1VERTEPORFIN

filter Dosage Reset all filters

322 All

01 2AEROSOL, METERED;INHALATION

02 2CAPSULE, DELAYED RELEASE;ORAL

03 11CAPSULE, EXTENDED RELEASE;ORAL

04 12CAPSULE;ORAL

05 25CREAM;TOPICAL

06 1FILM, EXTENDED RELEASE;TRANSDERMAL

07 1FOR SOLUTION;INHALATION

08 1FOR SOLUTION;OPHTHALMIC

09 3GEL;OPHTHALMIC

10 7GEL;RECTAL

11 13GEL;TOPICAL

12 1GEL;VAGINAL

13 1IMPLANT;IMPLANTATION

14 1IMPLANT;INTRAVITREAL

15 19INJECTABLE;INJECTION

16 1INJECTABLE;INTRAVITREAL

17 1INJECTABLE;SUBCUTANEOUS

18 1INSERT;OPHTHALMIC

19 8LOTION;TOPICAL

20 17OINTMENT;OPHTHALMIC

21 7OINTMENT;TOPICAL

22 1SHAMPOO;TOPICAL

23 2SOLUTION, GEL FORMING/DROPS;OPHTHALMIC

24 70SOLUTION/DROPS;OPHTHALMIC

25 1SOLUTION/DROPS;OPHTHALMIC, OTIC

26 6SOLUTION/DROPS;OTIC

27 4SOLUTION;INHALATION

28 1SOLUTION;INTRAOCULAR

29 1SOLUTION;INTRAVENOUS

30 1SOLUTION;OPHTHALMIC

31 1SOLUTION;ORAL

32 9SOLUTION;TOPICAL

33 6SPRAY, METERED;NASAL

34 12SUSPENSION/DROPS;OPHTHALMIC

35 3SUSPENSION/DROPS;OTIC

36 1SUSPENSION;INJECTION

37 4SUSPENSION;ORAL

38 1SYRUP;ORAL

39 22TABLET, EXTENDED RELEASE;ORAL

40 1TABLET, ORALLY DISINTEGRATING;ORAL

41 40TABLET;ORAL

filter Dosage Strength Reset all filters

322 All

01 10.005%

02 60.01%

03 10.01%;0.045%

04 10.01MG/SPRAY

05 10.02%

06 10.021MG/SPRAY

07 10.024%

08 60.025%

09 20.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML

10 10.025MG/SPRAY

11 10.02675%;0.315%

12 10.03%

13 10.04%

14 10.042MG/SPRAY

15 10.045%

16 10.06%

17 10.08%

18 110.1%

19 10.1%;0.3%

20 20.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

21 20.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

22 10.15%

23 10.15%;3.1%;1.2%

24 20.2%

25 10.2%;10%

26 10.25%

27 10.2MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

28 30.3%

29 10.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

30 10.38%

31 10.4%;0.3%

32 10.4MG/HR

33 170.5%

34 10.5%;0.3%

35 30.5%;10%

36 10.59MG

37 10.5MG

38 10.5MG/SPRAY

39 10.75%

40 171%

41 61%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

42 11.2%;0.025%

43 11.25MG

44 11.338GM/ML

45 21.5%

46 11.5MG

47 710%

48 110%;10% (5GM/50ML;5GM/50ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

49 110,000 UNITS/ML;EQ 1MG BASE/ML

50 2100,000 UNITS/GM;0.1%

51 1100,000 UNITS/ML

52 1100MG

53 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

54 1100MG/AMP

55 1100MG/ML

56 310MG

57 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

58 110MG/2ML (5MG/ML)

59 110MG/2ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

60 110MG/ML

61 110MG;25MG

62 112.5MG

63 4120MG

64 1125MG

65 1145MG

66 115%

67 1150MG

68 115MG/3ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

69 215MG/VIAL

70 1174MG

71 4180MG

72 21MG

73 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

74 42%

75 22%;0.79%

76 12%;1%

77 22.5%

78 12.5%;EQ 1.2% BASE

79 12.5MG

80 12.5MG/0.5ML (5MG/ML)

81 1200 UNITS/VIAL

82 1200MG

83 1200MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

84 120MG

85 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

86 120MG/4ML (5MG/ML)

87 120MG/4ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

88 120MG/VIAL

89 3240MG

90 4250MG

91 525MG

92 225MG/ML

93 12MG

94 13.75%

95 13.75%;EQ 1.2% BASE

96 130%

97 4300MG

98 130MG

99 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

100 1348MG

101 135MG

102 3360MG

103 1385MG;30MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

104 14%

105 14.5MG

106 2400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

107 1400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM

108 2400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

109 1400MG

110 140MG

111 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

112 140MG/ML

113 2420MG

114 148MG

115 35%

116 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

117 15%;1%

118 25%;EQ 1% BASE

119 15.2MG/SPRAY

120 1500 UNITS/GM

121 2500 UNITS/GM;10,000 UNITS/GM

122 2500MG

123 1500MG/ML

124 250MG

125 250MG/ML

126 1522MG

127 35MG

128 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

129 15MG/GM

130 15MG/ML

131 15MG/ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

132 15MG;12.5MG

133 15MG;2.5MG

134 16,200 UNITS/VIAL

135 260MG

136 160MG/5ML

137 16GM/VIAL

138 1770MG;60MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

139 190MG

140 3EQ 0.025% BASE

141 1EQ 0.05% PHOSPHATE

142 1EQ 0.07% ACID

143 1EQ 0.083% BASE

144 2EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

145 6EQ 0.1% BASE

146 2EQ 0.1% PHOSPHATE

147 2EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

148 2EQ 0.11% PHOSPHATE

149 1EQ 0.2% BASE

150 1EQ 0.23% PHOSPHATE;10%

151 4EQ 0.25% BASE

152 2EQ 0.2MG BASE/INH

153 2EQ 0.3% BASE

154 1EQ 0.3MG ACID/0.09ML

155 6EQ 0.5% BASE

156 1EQ 0.6% BASE

157 2EQ 0.9% PHOSPHATE

158 1EQ 1% BASE

159 2EQ 100MG BASE

160 1EQ 105MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

161 1EQ 115MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

162 1EQ 135MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

163 1EQ 15MG BASE/5ML

164 1EQ 1GM BASE/3ML

165 1EQ 2% BASE

166 1EQ 2% BASE;EQ 0.5% BASE

167 1EQ 200MG BASE/5ML

168 1EQ 3MG BASE/GM

169 1EQ 400MG BASE/5ML

170 1EQ 40MG BASE/ML

171 1EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

172 1EQ 500MG BASE/2ML

173 1EQ 50MG BASE

174 1EQ 50MG BASE/5ML

175 1EQ 50MG BASE/VIAL

176 1EQ 55MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

177 1EQ 65MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

178 1EQ 75MG BASE

179 1EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

180 1EQ 75MG BASE/2ML

181 1EQ 80MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

182 1EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

filter Regulatory Info Reset all filters

322 All

01 155DISCN

02 8OTC

03 156RX

04 3Blank

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01

Brand Name : ACETIC ACID 2% IN AQ...

FNCE

Not Confirmed

Brand Name : ACETIC ACID 2% IN AQ...

FNCE

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RLD : No

TE Code :

ACETIC ACID, GLACIAL; ALUMINUM ACETATE

Bausch & Lomb Incorporated

Dosage Form : SOLUTION/DROPS; OTIC

Proprietary Name : ACETIC ACID 2% IN AQUEOU...

Dosage Strength : 2%;0.79%

Approval Date : 1994-02-25

Application Number : 40063

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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02

Brand Name : BOROFAIR

FNCE

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Brand Name : BOROFAIR

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RLD : No

TE Code :

ACETIC ACID, GLACIAL; ALUMINUM ACETATE

Bausch & Lomb Incorporated

Dosage Form : SOLUTION/DROPS; OTIC

Proprietary Name : BOROFAIR

Dosage Strength : 2%;0.79%

Approval Date : 1985-08-21

Application Number : 88606

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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03

Brand Name : HYDROCORTISONE AND A...

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Brand Name : HYDROCORTISONE AND A...

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RLD : No

TE Code :

ACETIC ACID, GLACIAL; HYDROCORTISONE

Bausch & Lomb Incorporated

Dosage Form : SOLUTION/DROPS; OTIC

Proprietary Name : HYDROCORTISONE AND ACETI...

Dosage Strength : 2%;1%

Approval Date : 1994-10-31

Application Number : 40097

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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04

Brand Name : MIOCHOL-E

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Brand Name : MIOCHOL-E

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RLD : Yes

TE Code :

ACETYLCHOLINE CHLORIDE

Bausch & Lomb Incorporated

Dosage Form : FOR SOLUTION; OPHTHALMIC

Proprietary Name : MIOCHOL-E

Dosage Strength : 20MG/VIAL

Approval Date : 1993-09-22

Application Number : 20213

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
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05

Brand Name : ZOVIRAX

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Brand Name : ZOVIRAX

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RLD : Yes

TE Code : AB

Bausch & Lomb Incorporated

Dosage Form : OINTMENT; TOPICAL

Proprietary Name : ZOVIRAX

Dosage Strength : 5%

Approval Date : 1982-03-29

Application Number : 18604

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
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06

Brand Name : ZOVIRAX

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Brand Name : ZOVIRAX

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RLD : Yes

TE Code : AB

Bausch & Lomb Incorporated

Dosage Form : CREAM; TOPICAL

Proprietary Name : ZOVIRAX

Dosage Strength : 5%

Approval Date : 2002-12-30

Application Number : 21478

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
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07

Brand Name : XERESE

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Brand Name : XERESE

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RLD : Yes

TE Code :

ACYCLOVIR; HYDROCORTISONE

Bausch & Lomb Incorporated

Dosage Form : CREAM; TOPICAL

Proprietary Name : XERESE

Dosage Strength : 5%;1%

Approval Date : 2009-07-31

Application Number : 22436

RX/OTC/DISCN : RX

RLD : Yes

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08

Brand Name : CABTREO

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Brand Name : CABTREO

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RLD : Yes

TE Code :

ADAPALENE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE

Bausch & Lomb Incorporated

Dosage Form : GEL; TOPICAL

Proprietary Name : CABTREO

Dosage Strength : 0.15%;3.1%;1.2%

Approval Date : 2023-10-20

Application Number : 216632

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
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09

Brand Name : ALBUTEROL SULFATE

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Brand Name : ALBUTEROL SULFATE

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RLD : No

TE Code :

ALBUTEROL SULFATE

Bausch & Lomb Incorporated

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.5% BASE

Approval Date : 1998-06-18

Application Number : 75050

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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10

Brand Name : ALBUTEROL SULFATE

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Brand Name : ALBUTEROL SULFATE

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RLD : No

TE Code :

ALBUTEROL SULFATE

Bausch & Lomb Incorporated

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.083% BASE

Approval Date : 2000-03-29

Application Number : 75358

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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1
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Last

Contact Bausch & Lomb Incorporated and get a quotation

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 GREENVILLE, SOUTH CAROLINA. bulk offered by Bausch & Lomb Incorporated

Find a price of MANUFACTURING SITE,FACILITIES,PERSONNEL AND GENERAL OPERATING PROCEDURES IN TAMPA,FLORIDA. bulk offered by Bausch & Lomb Incorporated

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