Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 7Sanofi
02 1Allergan Aesthetics
03 3Actavis Inc
04 2Ailex Pharma
05 2Alfasigma
06 1Apotex Inc
07 1Appasamy Associates
08 1Aurobindo Pharma Limited
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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 1Eye Drop
11 1Eye Drop In Solution In Single-Dose Container
12 1Eye Drop Solution
13 2Eye Drops
14 2Eye Solution
15 4Eye drops, resolution
16 1Eye/Nasal Drops
17 2Hard Capsule
18 1Inhalation Powder
19 1NAS
20 1NASAL SOLUTION
21 3Nasal Spray
22 1Nose spray
23 1Nose spray, resolution
24 1OPD
25 4Ophthalmic Solution
26 2SOLUTION
27 6SOLUTION/DROPS;OPHTHALMIC
28 12SOLUTION;INHALATION
29 5SPRAY, METERED;NASAL
30 12Blank
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01 2Authorized
02 2Cancelled
03 20DISCN
04 2File-Available
05 6Generic
06 1NON-PRESCRIPTION DRUGS
07 1OTC
08 2Prescription
09 10RX
10 34Blank
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01 1ALLER-NIL
02 1Aurocrome
03 1Brunicrom
04 2CLESIN
05 1CROLOM
06 1CROMOLYN EYE DROPS
07 22CROMOLYN SODIUM
08 2CROMOPTIC
09 1Chromosome
10 1Cromabak
11 1CromoHexal
12 1Cromolyn Sodium
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14 1Cromostil Eye Drops
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17 2EYECROL
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20 2GASTROCROM
21 3Gastrofrenal
22 1Gastrofrenal 500
23 3INTAL
24 2Lecrolyn
25 1Lexumin
26 5Lomudal
27 2Lomudal Nasal
28 1Mirocrom
29 1NALCROM
30 1NASALCROM
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16 31USA
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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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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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
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
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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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
