EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI
02 14Sanofi
03 1Allergan Aesthetics
04 3Actavis Inc
05 1Adcock Ingram
06 2Ailex Pharma
07 1Apofri AB
08 1Apotex Inc
09 1Appasamy Associates
10 1Aurobindo Pharma Limited
11 1Aurolab
12 4Bausch & Lomb Incorporated
13 1Bruschettini
14 1FDC
15 2Farmak JSC
16 1GENERA PHARMS
17 1HH AND P
18 2Hanlim Pharmaceuticals Inc
19 1Hikma Pharmaceuticals
20 3ITALCHIMICI SpA
21 1Laboratoires Thea
22 2MARVECSPHARMA SERVICES Srl
23 1MC Pharma
24 2Micro Labs Limited
25 1Mirpharm
26 6ORIFARM GROUP AS
27 1PENDOPHARM DIVISION OF DE PHARMASCIENCE INC
28 2Pannon
29 2Paranova Group AS
30 1Perrigo Company plc
31 3Pfizer Inc
32 1Pharmascience Inc.
33 1Prestige Consumer Healthcare
34 1ROXANE
35 1Raha Pharmaceutical Co
36 1Rekah Pharmaceutical
37 1Rising Pharmaceuticals Inc
38 1SIFI
39 3Sandoz B2B
40 6Santen Pharmaceutical
41 1ScieGen Pharmaceuticals
42 1Teva Pharmaceutical Industries
43 1UCB Pharma S.A
44 1URSAPHARM Arzneimittel GmbH
45 2Unither Pharmaceuticals
46 1VIATRIS SPECIALTY
47 1VIRTUS PHARM
48 1Winston Medical Supply
49 1Wockhardt
50 4World Medicine
51 1Blank
01 1AEROSOL, METERED;INHALATION
02 1CAPSULE
03 1CAPSULE;INHALATION
04 1CAPSULE;ORAL
05 5CONCENTRATE;ORAL
06 1Capsule
07 1Drops
08 1EYE DROP
09 4EYE DROPS
10 5EYE DROPS, SOLUTION
11 3EYE DROPS, SOLUTION IN SINGLE-DOSE CONTAINERS
12 1Eye Drop
13 2Eye Drops
14 2Eye Solution
15 4Eye drops, resolution
16 1Gtt Opht
17 2INHALATION POWDER, HARD CAPSULE
18 3INHALATION, SUSPENSION
19 1NAS
20 1NASAL SOLUTION
21 5NASAL SPRAY, SOLUTION
22 3Nasal Spray
23 1Nose spray
24 1Nose spray, resolution
25 5OPD
26 1ORAL SOLUTION
27 2Ophthalmic Solution
28 2SOLUTION
29 6SOLUTION/DROPS;OPHTHALMIC
30 12SOLUTION;INHALATION
31 5SPRAY, METERED;NASAL
32 13Blank
01 20DISCN
02 2File-Available
03 8Generic
04 2OTC
05 2Originator
06 2Prescription
07 10RX
08 51Blank
01 1ALLER-NIL
02 1Allergo Comod
03 1Allgil
04 1Aurocrome
05 1BAUSCH & LOMB VIVIDRIN EYE DROPS
06 1Brunicrom
07 2CLESIN
08 1CROLOM
09 1CROMOLYN EYE DROPS
10 22CROMOLYN SODIUM
11 2CROMOPTIC
12 1Cromabak
13 1Cromabak 2% Eye Drops
14 1Crominet
15 1CromoHexal
16 1Cromohexal Eye Drops
17 2Cromopharm
18 1Cromostil Eye Drops
19 1Cromozil
20 2EYECROL
21 2GASTROCROM
22 1Gastrofrenal
23 1Gastrofrenal 500
24 3INTAL
25 5Lecrolyn
26 1Lecrolyn sine
27 1Lexumin
28 12Lomudal
29 1Lomudal GI
30 2Lomudal Nasal
31 4Lomudal nasal
32 1Mirocrom
33 1NALCROM
34 1NASALCROM
35 3Nalcrom
36 1Nasal Lomusol
37 1OPTICROM
38 1PMS-SODIUM CROMOGLYCATE
39 1Rynacrom
40 1Sificrom
41 1Stop-Allerg Eye Drops
42 2Taleum
43 5Blank
01 1Australia
02 3Canada
03 2France
04 2Hungary
05 2India
06 1Iran
07 1Israel
08 12Italy
09 6Norway
10 1Russia
11 6South Africa
12 2South Korea
13 19Sweden
14 1Switzerland
15 1Taiwan
16 4Turkey
17 31USA
18 2Ukraine
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : INHALATION, SUSPENSION
Dosage Strength : 5 MG / DOSE
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : INTAL
Dosage Form : CAPSULE;INHALATION
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 16990
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OPTICROM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-10-03
Application Number : 18155
Regulatory Info : DISCN
Registration Country : USA
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal nasal
Dosage Form : NASAL SPRAY, SOLUTION
Dosage Strength : 2.6 MG / DOSE
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : EYE DROPS, SOLUTION IN SINGLE-DOSE CONTAINERS
Dosage Strength : 40 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : EYE DROPS, SOLUTION
Dosage Strength : 20 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : INHALATION POWDER, HARD CAPSULE
Dosage Strength : 20 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal GI
Dosage Form : ORAL SOLUTION
Dosage Strength : 20 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal nasal
Dosage Form : NASAL SPRAY, SOLUTION
Dosage Strength : 5.2 MG / DOSE
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Lomudal
Dosage Form :
Dosage Strength : Coll 10 Ml 4%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Lomudal
Dosage Form :
Dosage Strength : Nasal Soluz 30 Ml 4 % + Nebulizer
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Lomudal
Dosage Form :
Dosage Strength : 24 Vials 20 Mg 2 Ml Aerosol
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Norway
Brand Name : Lomudal
Dosage Form : Eye drops, resolution
Dosage Strength : 20 mg/ml
Packaging : Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Norway
Brand Name : Lomudal
Dosage Form : Eye drops, resolution
Dosage Strength : 40 mg/ml
Packaging : Pipette, endose
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Norway
Brand Name : Lomudal Nasal
Dosage Form : Nose spray, resolution
Dosage Strength : 5.2 mg/dose
Packaging : Bottle of white plastic
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : NALCROM
Dosage Form : CAPSULE
Dosage Strength : 100MG
Packaging : 100
Approval Date :
Application Number : 500895
Regulatory Info : Prescription
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Rynacrom
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 5.2MG/SPRAY
Packaging :
Approval Date : 2001-07-26
Application Number : 74800
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SOLUTION;INHALATION
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 1999-07-19
Application Number : 75067
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SOLUTION;INHALATION
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 1994-04-26
Application Number : 74209
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROLOM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 4%
Packaging :
Approval Date : 1995-01-30
Application Number : 74443
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : INTAL
Dosage Form : SOLUTION;INHALATION
Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-05-28
Application Number : 18596
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : INTAL
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.8MG/INH
Packaging :
Approval Date : 1985-12-05
Application Number : 18887
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOPTIC
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 4%
Packaging :
Approval Date : 1999-04-27
Application Number : 75088
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NASALCROM
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 5.2MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-01-03
Application Number : 20463
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SOLUTION;INHALATION
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 1999-09-30
Application Number : 75175
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 4%
Packaging :
Approval Date : 1998-04-29
Application Number : 74706
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CROMOLYN SODIUM
Dosage Form : SOLUTION;INHALATION
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 2000-01-18
Application Number : 75271
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : GASTROCROM
Dosage Form : CAPSULE;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 1989-12-22
Application Number : 19188
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : GASTROCROM
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 100MG/5ML
Packaging :
Approval Date : 1996-02-29
Application Number : 20479
Regulatory Info : RX
Registration Country : USA
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