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    Perrigo Company plc

    EVENTS

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    DIGITAL CONTENT

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    EXCIPIENTS

    REF. STANDARDS & IMPURITIES

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    01 4ACETAMINOPHEN

    02 1ACETAMINOPHEN; ASPIRIN; CAFFEINE

    03 1ACETAMINOPHEN; IBUPROFEN

    04 2ATORVASTATIN CALCIUM

    05 1Anhydrous Caffeine; Propiphenazone

    06 3Ascorbic Acid

    07 1Ascorbic Acid; Sodium Ascorbate

    08 1BACITRACIN

    09 3BETAMETHASONE DIPROPIONATE

    10 2BETAMETHASONE VALERATE

    11 1BRINZOLAMIDE;BRIMONIDINE TARTRATE

    12 1Beclomethasone Dipropionate

    13 2CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE

    14 8CETIRIZINE HYDROCHLORIDE

    15 2CIMETIDINE

    16 1CLEMASTINE FUMARATE

    17 1CROMOLYN SODIUM

    18 1Caffeine; Paracetamol

    19 3Calcium Carbonate

    20 1Chlorhexidine

    21 2Cholecalciferol; Retinol Palmitate

    22 1Choline salicylate

    23 1Codeine Phosphate Hemihydrate; Ibuprofen

    24 1Cucurbita Pepo L. Soft Seed Extract

    25 1Cyanocobalamin; Folic Acid Hydrate; Calcium Pantothenate; Nicotinamide; Pyridoxine Hydrochloride; Riboflavin; Thiamine Nitrate

    26 1DESLORATADINE

    27 2DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN

    28 2DICLOFENAC SODIUM

    29 1DIPHENHYDRAMINE CITRATE; IBUPROFEN

    30 5DIPHENHYDRAMINE HYDROCHLORIDE

    31 1DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

    32 1DOCUSATE SODIUM

    33 1DOXYLAMINE SUCCINATE

    34 1Diazepam

    35 2Diphenhydramine Hydrochloride

    36 1ERYTHROMYCIN

    37 1ESOMEPRAZOLE MAGNESIUM

    38 5FAMOTIDINE

    39 2FEXOFENADINE HYDROCHLORIDE

    40 1FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    41 2FLUOCINOLONE ACETONIDE

    42 1FLUOCINONIDE

    43 2GUAIFENESIN

    44 2GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE

    45 3Glycerol

    46 3Glycerol; Urea

    47 1HALOBETASOL PROPIONATE

    48 7HYDROCORTISONE

    49 1Hydrocortisone; Sodium Chloride; Urea

    50 15IBUPROFEN

    51 1IBUPROFEN SODIUM

    52 1IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE

    53 1IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

    54 1ISONIAZID

    55 3Ibuprofen

    56 1Iron(II) Sulfate Heptahydrate

    57 1KETOPROFEN

    58 1Kolekalciferol

    59 2LANSOPRAZOLE

    60 1LEVOCETIRIZINE DIHYDROCHLORIDE

    61 2LEVONORGESTREL

    62 4LOPERAMIDE HYDROCHLORIDE

    63 2LOPERAMIDE HYDROCHLORIDE; SIMETHICONE

    64 5LORATADINE

    65 2LORATADINE; PSEUDOEPHEDRINE SULFATE

    66 1Levonorgestrel

    67 1MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE

    68 2MEPROBAMATE

    69 7MICONAZOLE NITRATE

    70 1MINERAL OIL

    71 5MINOXIDIL

    72 1MOMETASONE FUROATE

    73 1MONTELUKAST SODIUM

    74 1Magnesium Hydroxide

    75 2Melatonin

    76 1Methyl Salicylates; Salicylic Acid; Racemic Camphor; Concentrated Formic Acid; Spike Ether Oil

    77 3NAPROXEN

    78 1NAPROXEN SODIUM

    79 1NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE

    80 20NICOTINE POLACRILEX

    81 2NITROFURAZONE

    82 1NYSTATIN

    83 2NYSTATIN; TRIAMCINOLONE ACETONIDE

    84 1Natriumklorid Urea

    85 26Nicotine

    86 27Nicotine Resinate

    87 1OMEPRAZOLE MAGNESIUM

    88 1OMEPRAZOLE; SODIUM BICARBONATE

    89 14Oxymetazoline Hydrochloride

    90 1PANTOPRAZOLE SODIUM

    91 1PENTOBARBITAL SODIUM

    92 1PERMETHRIN

    93 1PETROLATUM

    94 1PHENYLEPHRINE HYDROCHLORIDE

    95 3POLYETHYLENE GLYCOL 3350

    96 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    97 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE

    98 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    99 1POLYMYXIN B SULFATE

    100 1PSEUDOEPHEDRINE HYDROCHLORIDE

    101 7Paracetamol

    102 1Paracetamol; Caffeine

    103 1Paracetamol; Codeine Phosphate

    104 2Paracetamol; Codeine phosphate; Caffeine

    105 2Paracetamol; Codeine; Caffeine

    106 2Paracetamol; Guaifenesin; Phenylephrine

    107 1Paracetamol; Phenylephhrine Hydrochloride; Guaifenesin

    108 1Paracetamol; Phenylephrine Hydrochloride

    109 5Paracetamol; Phenylephrine; Ascorbic acid

    110 1Paracetamol; Phenylephrine; Terpin hydrate; Ascorbic acid; Caffeine

    111 8Penciclovir

    112 1Pencilclovir

    113 3Permethrin

    114 3Progesterone

    115 2Pyrantel

    116 1QUINIDINE SULFATE

    117 3RANITIDINE HYDROCHLORIDE

    118 1RRR-Alpha-Tocopheryl Acetate (Vitamin E acetate, natural stereoisomer)

    119 1SECOBARBITAL SODIUM

    120 2SILDENAFIL CITRATE

    121 1SUMATRIPTAN

    122 1Selegiline Hydrochloride

    123 4Simethicone

    124 3TESTOSTERONE

    125 1TESTOSTERONE UNDECANOATE

    126 1TIOCONAZOLE

    127 2TRIAMCINOLONE ACETONIDE

    128 2Tripelenamine Hydrochloride

    129 2Ulipristal Acetate

    130 3Urea

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    Brand Name : ACETAMINOPHEN

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    Regulatory Info : OTC

    Registration Country : USA

    ACETAMINOPHEN

    Perrigo Company plc

    Dosage Form : SUPPOSITORY;RECTAL

    Brand Name : ACETAMINOPHEN

    Dosage Strength : 120MG

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    Approval Date : 1987-04-06

    Application Number : 70607

    Regulatory Info : OTC

    Registration Country : USA

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    Perrigo Company plc

    Dosage Form : SUPPOSITORY;RECTAL

    Brand Name : ACETAMINOPHEN

    Dosage Strength : 650MG

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    Approval Date : 1986-12-01

    Application Number : 70608

    Regulatory Info : OTC

    Registration Country : USA

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    Perrigo Company plc

    Dosage Form : TABLET, EXTENDED RELEASE...

    Brand Name : ACETAMINOPHEN

    Dosage Strength : 650MG

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    Approval Date : 2000-02-25

    Application Number : 75077

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    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

    ACETAMINOPHEN

    Perrigo Company plc

    Dosage Form : TABLET (EXTENDED-RELEASE...

    Brand Name : ACETAMINOPHEN ARTHRITIS P...

    Dosage Strength : 650MG

    Packaging : 24/30/50/60/100/120/200

    Approval Date :

    Application Number : 2272482

    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

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    Regulatory Info : OTC

    Registration Country : USA

    ACETAMINOPHEN; ASPIRIN; CAFFEINE

    Perrigo Company plc

    Dosage Form : TABLET;ORAL

    Brand Name : ACETAMINOPHEN, ASPIRIN AN...

    Dosage Strength : 250MG;250MG;65MG

    Packaging :

    Approval Date : 2001-11-26

    Application Number : 75794

    Regulatory Info : OTC

    Registration Country : USA

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    Regulatory Info : OTC

    Registration Country : USA

    ACETAMINOPHEN; IBUPROFEN

    Perrigo Company plc

    Dosage Form : TABLET;ORAL

    Brand Name : ACETAMINOPHEN AND IBUPROF...

    Dosage Strength : 250MG;125MG

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    Approval Date : 2023-02-28

    Application Number : 214836

    Regulatory Info : OTC

    Registration Country : USA

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    Brand Name : Optalidon

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    Regulatory Info : Authorized

    Registration Country : Spain

    Anhydrous Caffeine; Propiphenazone

    Perrigo Company plc

    Dosage Form : Suppository

    Brand Name : Optalidon

    Dosage Strength : 500MG; 75MG

    Packaging :

    Approval Date : 01-12-1950

    Application Number : 14517

    Regulatory Info : Authorized

    Registration Country : Spain

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    Brand Name : Vitamin C

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Ascorbic Acid

    Aco Hud Nordic

    Dosage Form : Tablet

    Brand Name : Vitamin C

    Dosage Strength : 300mg

    Packaging :

    Approval Date : 02/03/1973

    Application Number : 19730302000047

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Brand Name : Vitamin C Sugar-Free...

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Ascorbic Acid

    Aco Hud Nordic

    Dosage Form : Effervescent Tablet

    Brand Name : Vitamin C Sugar-Free Oran...

    Dosage Strength : 1g

    Packaging :

    Approval Date : 03/02/1989

    Application Number : 19890203000130

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Brand Name : Vitamin C Sugar-Free...

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Ascorbic Acid

    Aco Hud Nordic

    Dosage Form : Effervescent Tablet

    Brand Name : Vitamin C Sugar-Free Lemo...

    Dosage Strength : 1g

    Packaging :

    Approval Date : 16/11/1979

    Application Number : 19791116000128

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.