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59 products match your search.
Acetaminophen Suppositories USP, 120 mg

Acetaminophen Suppositories USP, 650 mg

Ammonium Lactate Cream 12%

Ammonium Lactate Lotion 12%

Aspirin Suppositories, USP

Bacitracin

Benzoyl Peroxide 10% Acne Medication Wash

Benzoyl Peroxide 10% Aqueous Base, Acne Treatment Gel

Benzoyl Peroxide 2.5% Aqueous Base, Acne Treatment Gel

Benzoyl Peroxide 5% Acne Medication Wash

Benzoyl Peroxide 5% Aqueous Base, Acne Treatment Gel

Bisacodyl Suppositories, USP 10 mg
Compare to the Active Ingredient of: DULCOLAX®
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride Extended Release Tablets, 5mg/120mg
Compare to the Active Ingredient of: Zyrtec-D®
Cetirizine Hydrochloride Tablets, 10 mg
Compare to the Active Ingredient of: Zyrtec®
Children's Acetaminophen Oral Suspension 160 mg per 5 mL Cherry Flavor
Compare to the Active Ingredient of: Children's Tylenol® Oral Suspension
Children's Acetaminophen Oral Suspension 160 mg per 5 mL Grape Flavor
Compare to the Active Ingredient of: Children's Tylenol® Oral Suspension
Children's Cetirizine Hydrochloride Oral Solution 1mg/mL
Compare to the Active Ingredient of: Children's Zyrtec®
Children's Ibuprofen Oral Suspension 100 mg per 5 mL (teaspoonful) Berry Flavor
Compare to the Active Ingredient of: Children's Motrin®
Children's Ibuprofen Oral Suspension 100 mg per 5 mL (teaspoonful) Grape Flavor
Compare to the Active Ingredient of: Children's Motrin®
Children's Ibuprofen Oral Suspension 100 mg per 5 mL Bubble Gum Flavor
Compare to the Active Ingredient of: Children's Motrin®
Clotrimazole Cream USP, 1%
Compare to the Active Ingredient of: Lotrimin® AF
Compound Benzoin Tincture USP

Dextromethorphan Polistirex Extended-Release Oral Suspension
Compare to the Active Ingredient of: Delsym®
Dibucaine Ointment 1%
Compare to the Active Ingredient of: Nupercainal®
Diphenhydramine HCl And Zinc Acetate Cream
Compare to the Active Ingredients of: Extra Strength Benadryl® Cream
Docusate Sodium
Compare to the Active Ingredient of: Colace®
Ferrous Gluconate Tablets, USP 324 mg

Ferrous Sulfate Enteric-Coated Tablets 324 mg

Fexofenadine Hydrochloride Tablets, 180 mg
Compare to the Active Ingredient of: Allegra® Allergy
Fexofenadine Hydrochloride Tablets, 60 mg
Compare to the Active Ingredient of: Allegra® Allergy
Fluticasone Propionate (Glucocorticoid) 50 mcg per spray
Compare to the Active Ingredient of: Flonase® Allergy Relief
Guaifenesin and Pseudoephedrine Hydrochloride Extended-Release Tablets, 600 mg/60 mg
Compare to the Active Ingredients of: Mucinex® D
Hemorrhoidal Ointment
Compare to the Active Ingredients of: Preparation H® Ointment
Hydrocortisone 1% Ointment
Compare to the Active Ingredient of: Cortizone•10®
Hydrocortisone Cream 1%
Compare to the Active Ingredient of: Cortaid®
Infants' Concentrated Drops Ibuprofen Oral Suspension 50 mg per 1.25 mL Berry Flavor
Compare to the Active Ingredient of: Motrin® Infants' Drops
Isopropyl Rubbing Alcohol 70% USP

Lansoprazole Delayed-Release Capsules, 15mg
Compare to the Active Ingredient of: Prevacid® 24HR
Loratadine Tablets, 10 mg
Compare to the Active Ingredient of: Claritin®
Loratadine-D 12 Hour Pseudoephedrine Sulfate 120 mg/Loratadine 5 mg Extended Release Tablets
Compare to the Active Ingredient of: Claritin-D® 12 Hour
Mineral Oil USP

Muscle Rub
Compare to the Active Ingredients of: Bengay®
Naproxen Sodium Tablets 220 mg
Compare to the Active Ingredient of: Aleve®
Nicotine Polacrilex Gum 2 mg (nicotine) Mint Flavor
Compare to the Active Ingredient of: Nicorette® Gum
Nicotine Polacrilex Gum 4 mg (nicotine) Mint Flavor
Compare to the Active Ingredient of: Nicorette® Gum
Nicotine Polacrilex Lozenge 2 mg (nicotine) Mini Lozenge
Compare to the Active Ingredient of: Nicorette® Mini Lozenge
Nicotine Polacrilex Lozenge 2 mg (nicotine) Mint Flavor
Compare to the Active Ingredient of: Nicorette® Lozenge
Nicotine Polacrilex Lozenge 4 mg (nicotine) Mini Lozenge
Compare to the Active Ingredient of: Nicorette® Mini Lozenge
Nicotine Polacrilex Lozenge 4 mg (nicotine) Mint Flavor
Compare to the Active Ingredient of: Nicorette® Lozenge
Omeprazole Delayed Release Tablets 20mg

Oxymetazoline HCl 0.05%
Compare to the Active Ingredient of: Afrin®
Polyethylene Glycol 3350
Compare to the Active Ingredient of: MiraLAX®
Pseudoephedrine Hydrochloride 30 mg
Compare to the Active Ingredient of: Sudafed® Congestion
Pseudoephedrine Hydrochloride Extended-Release Tablets 120 mg
Compare to the Active Ingredient of: Sudafed® 12 Hour
Saline Nasal Spray
Compare to: Ocean® Ingredients
Triamcinolone Acetonide (Glucocorticoid) 55 mcg per spray
Compare to the Active Ingredient of: Nasacort® Allergy 24 HR
Triple Antibiotic Ointment
Compare to the Active Ingredients of: Neosporin®
Trolamine Salicylate 10%
Compare to the Active Ingredient of: Aspercreme®
Vitamin A and D Ointment
Compare to the Active Ingredients of: A+D® Original Ointment
Important Safety Information
  • Alogliptin is contraindicated in patients with a history of serious hypersensitivity reaction to alogliptin-containing products such as anaphylaxis, angioedema, or severe cutaneous adverse reactions.
  • Acute pancreatitis: There have been postmarketing reports of acute pancreatitis. If pancreatitis is suspected, promptly discontinue Alogliptin.
  • Hypersensitivity: There have been postmarketing reports of serious hypersensitivity reactions in patients treated with Alogliptin such as anaphylaxis, angioedema or severe cutaneous adverse reactions. In such cases, promptly discontinue Alogliptin, assess for other potential causes, institute appropriate monitoring and treatment, and initiate alternative treatment for diabetes. Use caution in a patient with a history of angioedema with another DPP-4i because it is unknown whether such patients will be predisposed to angioedema.
  • Hepatic effects: Postmarketing reports of hepatic failure, sometimes fatal. Causality cannot be excluded. Baseline liver test panel is recommended. If liver injury is detected, promptly interrupt Alogliptin and assess patient for probable cause, then treat cause if possible, to resolution or stabilization. Do not restart Alogliptin if liver injury is confirmed and no alternative etiology can be found.
  • Hypoglycemia: Insulin and insulin secretagogues are known to cause hypoglycemia. A lower dose of the insulin or insulin secretagogue may be required to minimize the risk when used in combination with Alogliptin.
  • Arthralgia: Severe and disabling arthralgia has been reported in patients taking DPP-4 inhibitors. Consider as a possible cause for severe joint pain and discontinue drug if appropriate.
  • Macrovascular outcomes: There have been no clinical studies establishing conclusive evidence of macrovascular risk reduction with Alogliptin or any other anti-diabetic drug.
  • Most common adverse reactions (4% of patients treated with Alogliptin 25 mg and more frequently than in patients who received placebo) were nasopharyngitis (4.4%), headache (4.2%), and upper respiratory tract infection (4.2%).

Patients taking Alogliptin should contact their health care professionals right away if they develop signs and symptoms of heart failure such as:

  • Unusual shortness of breath during daily activities
  • Trouble breathing when lying down
  • Tiredness, weakness, or fatigue
  • Weight gain with swelling in the ankles, feet, legs, or stomach Patients should not stop taking their medicine without first talking to their health care professionals.

Patients should not stop taking their medicine without first talking to their health care professionals.

Indication

Alogliptin is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Alogliptin is not for treatment of type 1 diabetes or diabetic ketoacidosis.

Please see Full Prescribing Information, including Medication Guide for Alogliptin.


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