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Latest Content by PharmaCompass
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01 2ACITRETIN
02 2ASPIRIN; BUTALBITAL; CAFFEINE
03 1ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
04 2Atropine
05 1BEZAFIBRATE
06 2BRIMONIDINE TARTRATE
07 5Bimatoprost
08 1Bismuth Subcitrate Potassium; Metronidazole; Tetracycline Hydrochloride
09 1Brimonidine Tartrate
10 1Brimonidine Tartrate; Timolol
11 2CHLORAMPHENICOL
12 1CHLORAMPHENICOL; PREDNISOLONE
13 1CROMOLYN SODIUM
14 1CYCLOSPORINE
15 1Carmelose Sodium
16 1Cyclopentolate
17 1DEXAMETHASONE
18 2DICYCLOMINE HYDROCHLORIDE
19 3DILTIAZEM HYDROCHLORIDE
20 1DIPIVEFRIN HYDROCHLORIDE
21 3Dexamethasone
22 1EPINASTINE HYDROCHLORIDE
23 4ETHINYL ESTRADIOL; NORETHINDRONE
24 1ETHOXZOLAMIDE
25 2Eluxadolin
26 2Eluxadoline
27 1Epinastine
28 4FLUOCINOLONE ACETONIDE
29 1FLUOROMETHOLONE
30 1FLUOROMETHOLONE; SULFACETAMIDE SODIUM
31 1FLURBIPROFEN SODIUM
32 1Flurbiprofen
33 1GATIFLOXACIN
34 1GENTAMICIN SULFATE
35 2GENTAMICIN SULFATE; PREDNISOLONE ACETATE
36 5HYDROCORTISONE
37 2HYDROXYPROGESTERONE CAPROATE
38 1IDOXURIDINE
39 1IRON DEXTRAN
40 1KETOROLAC TROMETHAMINE
41 2Ketorolac Tromethamine
42 1Ketorolaco Trometamol
43 2LEVOBUNOLOL HYDROCHLORIDE
44 6LIOTRIX (T4;T3)
45 3Levobunolol
46 2Levobunolol hydrochloride
47 1MEDRYSONE
48 1MEMANTINE HYDROCHLORIDE
49 12MORPHINE SULFATE
50 1NAPHAZOLINE HYDROCHLORIDE
51 4NEBIVOLOL HYDROCHLORIDE
52 1NEDOCROMIL SODIUM
53 1NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE
54 1OFLOXACIN
55 2OXYBUTYNIN
56 2Ofloxacin
57 5OnabotulinumtoxinA
58 1PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE
59 1PODOFILOX
60 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE
61 2PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
62 1PROPARACAINE HYDROCHLORIDE
63 4Pancreas Powder
64 2Pilocarpine
65 1SELENIUM SULFIDE
66 3SULFACETAMIDE SODIUM
67 2Sodium Carmellose
68 2TRETINOIN
69 1TRIAMCINOLONE ACETONIDE
70 3TRIMEPRAZINE TARTRATE
71 2TROSPIUM CHLORIDE
72 2Tazaroten
73 4Tazarotene
74 1Timolol Maleate; Brimonidine
75 2Timolol; Bimatoprost
76 1Timolol; Brimonidine
77 1pirenoxine
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01 87ALLERGAN
02 14ALLERGAN HERBERT
03 3ALLERGAN INC
04 1ALLERGAN PHARMACEUT.INTERN.LTD
05 8ALLERGAN PHARMACEUTIC.IRELAND
06 14ALLERGAN SpA
07 1Allergan France
08 1Allergan Limited
09 4Allergan Pharmaceuticals (Pty) Ltd
10 4Allergan Pharmaceuticals International Limited
11 6Allergan Pharmaceuticals International Ltd
12 9Allergan Pharmaceuticals Ireland
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01 2AEROSOL;TOPICAL
02 1Bimatoprost 0,3Mg/Ml 0.4 Ml 30Units Solution Ophthalmic Use
03 1Bimatoprost 0,3Mg/Ml 3Ml Solution Ophthalmic Use
04 1Bimatoprost 0.1Mg/Ml 3Ml Solution Ophthalmic Use
05 1Bismuth Oxide+Metronidazole+Tetracycline Hydrochloride 140+125+125Mg 120 Unita' Oral Use
06 1Brimonidine 0.2% 5Ml Solution Ophthalmic Use
07 2CAPSULE
08 17CAPSULE, EXTENDED RELEASE;ORAL
09 3CAPSULE;ORAL
10 4CREAM;TOPICAL
11 4Capsule
12 1Dexamethasone 700Mcg 1 Units Use Intravitreale
13 1EMULSION; OPHTHALMIC
14 3Eye Drop
15 2Eye Drop In Solution In Single-Dose Container
16 3Eye Drop Solution
17 1FILM, EXTENDED RELEASE;TRANSDERMAL
18 4Film Coated Tablet
19 2GEL
20 1GEL, METERED;TRANSDERMAL
21 3GEL;TOPICAL
22 4Gel
23 3INJECTABLE;INJECTION
24 1INJECTABLE;INTRA-ARTICULAR, INTRAMUSCULAR, INTRAVITREAL
25 1LOTION/SHAMPOO;TOPICAL
26 1Levobunolol 0.5% 0.4 Ml 60 Units Solution Ophthalmic Use
27 1Levobunolol 0.5% 5Ml Solution Ophthalmic Use
28 6OINTMENT;OPHTHALMIC
29 2OINTMENT;TOPICAL
30 2OPD
31 21SOLUTION/DROPS;OPHTHALMIC
32 1SOLUTION;ORAL
33 2SOLUTION;TOPICAL
34 3SUSPENSION/DROPS;OPHTHALMIC
35 2SUSPENSION;OPHTHALMIC
36 1SYRUP;ORAL
37 1Solution
38 1TABLET (EXTENDED-RELEASE)
39 15TABLET;ORAL
40 2TABLET;ORAL-21
41 2TABLET;ORAL-28
42 1Timolol+Bimatoprost 300Mcg/Ml+5Mg/Ml 30 Joined' Solution Ophthalmic Use
43 1Timolol+Bimatoprost 900Mcg+15Mg Solution Ophthalmic Use
44 1Timolol+Bromonidine 0.2%+0.5% 5Ml Solution Ophthalmic Use
45 5VIAL; SINGLE-USE
46 14Blank
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01 10.0005
02 10.001
03 10.01%
04 10.01% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.0125MG;0.0031MG
06 30.025%
07 10.025MG;0.0063MG
08 10.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 20.035MG;0.5MG
10 20.035MG;1MG
11 10.0375%
12 20.05%
13 10.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 10.05MG;0.0125MG
15 10.075%
16 30.1%
17 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 10.1%;10%
19 10.10%
20 10.12%;0.1%
21 10.15MG;0.0375MG
22 10.1MG
23 10.1MG;0.025MG
24 10.2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 20.2%;10%
26 10.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 10.25MG;0.0625MG
28 10.3%
29 10.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 10.3MG
31 60.5%
32 10.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 51%
34 11%;0.5%
35 210%
36 110,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 2100 UNITS/VIAL
38 110000U
39 2100MG
40 1100mg
41 210MG
42 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
43 1120 cps 140 mg + 125 mg + 125 mg
44 1120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1125MG
46 1125MG/ML
47 1130MG
48 1150MG
49 1180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 11mg/g
51 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 22.5%
53 1200 UNITS/VIAL
54 1200MG
55 120MG
56 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 1240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
58 125000U
59 1250MG/ML
60 125MG
61 12MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 12MG/ML; 5MG/ML
63 12MG; 5 MG
64 13%
65 13.9MG/24HR
66 130%
67 130MG
68 2325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1325MG;50MG;40MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 14% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
71 140 Monod Coll 0.4 Ml 0.03%
72 140000U
73 1400MG
74 140MG
75 250 UNITS/VIAL
76 15000U
77 150MG
78 15MG
79 15MG/ML
80 55mg/ml
81 160MG
82 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
83 170MG
84 175MG
85 175mg
86 180MG
87 18MG/0.1ML (8MG/0.1ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
88 1Coll 10 Ml 0.3%
89 1Coll 10 Ml 0.5%
90 2Coll 10 Ml 1%
91 1Coll 10 Ml 2%
92 1Coll 3 Ml 0.2%
93 1Coll 3 Ml 1%
94 1Coll 5 Ml 0,5 Mg/Ml
95 1Coll 5 Ml 0.1%
96 1Coll 5 Ml 0.5%
97 1Coll Bottle Groun 0.005% + Plug Solv 7 Ml
98 1EQ 0.3% BASE
99 1EQ 0.3% BASE;0.6%
100 1EQ 0.3% BASE;1%
101 1EQ 0.35% BASE;10,000 UNITS/ML;0.5%
102 1EQ 100MG IRON/2ML (EQ 50MG IRON/ML)
103 1EQ 10MG BASE
104 2EQ 2.5MG BASE
105 1EQ 2.5MG BASE/5ML
106 1EQ 20MG BASE
107 2EQ 5MG BASE
108 1EYE DROPS 3 ML 300 mcg/ml + 5 mg/ml
109 1EYE DROPS 3 ml 0,3 mg/ml
110 1EYE DROPS 3 ml 0. 1 mg/ml
111 1EYE DROPS 5 ml 0.2% + 0.5%
112 1EYE DROPS 5 ml 2 mg/ml
113 1EYE DROPS 5 ml 5 mg/ml
114 1Pom Oftalm 3,5 G 0,3%
115 1Ung Oftalm 3 G 0,2%
116 1collyrium 30 monodose containers 0.4 ml 300 mcg/ml + 5 mg/ml
117 1collyrium 30 monodose vials 0.4 ml 0,3 mg/ml
118 1collyrium 60 monodose vials 0.4 ml 5 mg/ml
119 1intravitreale implant 700 mcg + applicator
120 1Blank
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01 3Canada
02 25Italy
03 2Malta
04 4South Africa
05 9Spain
06 10Sweden
07 99USA
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : CAPSULE
Brand Name : SORIATANE
Dosage Strength : 25MG
Packaging : 30
Approval Date :
Application Number : 2070863
Regulatory Info : PRESCRIPTION
Registration Country : Canada
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : CAPSULE
Brand Name : SORIATANE
Dosage Strength : 10MG
Packaging : 30
Approval Date :
Application Number : 2070847
Regulatory Info : PRESCRIPTION
Registration Country : Canada
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FIORINAL
Dosage Strength : 325MG;50MG;40MG **Fede...
Packaging :
Approval Date : 1986-04-16
Application Number : 17534
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : FIORINAL
Dosage Strength : 325MG;50MG;40MG **Fede...
Packaging :
Approval Date : 1986-04-16
Application Number : 17534
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Dosage Form : CAPSULE;ORAL
Brand Name : FIORINAL W/CODEINE
Dosage Strength : 325MG;50MG;40MG;30MG *...
Packaging :
Approval Date : 1990-10-26
Application Number : 19429
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info :
Registration Country : Italy
Dosage Form :
Brand Name : Atropine Lux
Dosage Strength : Coll 10 Ml 0.5% ...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info :
Registration Country : Italy
Dosage Form :
Brand Name : Atropine Lux
Dosage Strength : Coll 10 Ml 1% ...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET (EXTENDED-RELEASE...
Brand Name : BEZALIP SR
Dosage Strength : 400MG
Packaging : 30
Approval Date :
Application Number : 2083523
Regulatory Info : PRESCRIPTION
Registration Country : Canada
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Regulatory Info :
Registration Country : Italy
Dosage Form : Bimatoprost 0.1Mg/Ml 3Ml...
Brand Name : Lumigan
Dosage Strength : EYE DROPS 3 ml 0. 1 mg...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info :
Registration Country : Italy
Dosage Form : Bimatoprost 0,3Mg/Ml 3Ml...
Brand Name : Lumigan
Dosage Strength : EYE DROPS 3 ml 0,3 mg/...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Allergan Aesthetics is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of Botulinum toxin type A bulk offered by Allergan Aesthetics