Aurobindo Receives FDA Approval for Aripiprazole Orally Disintegrating Tablets USP, 10 mg and 15 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Aripiprazole Orally Disintegrating Tablets USP, 10 mg and 15 mg. Aurobindo Pharma’s Aripiprazole Orally Disintegrating Tablets USP, are an AB-rated generic equivalent to the reference listed drug (RLD), Abilify Discmelt® Orally Disintegrating […]

Aurobindo Receives FDA Approval for Aripiprazole Orally Disintegrating Tablets USP, 10 mg and 15 mg Read More »

Aurobindo Receives FDA Approval for Betamethasone Dipropionate Cream USP, 0.05%

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Betamethasone Dipropionate Cream USP, 0.05%. Aurobindo Pharma’s Betamethasone Dipropionate Cream USP, are an AB-rated generic equivalent to the reference listed drug (RLD), Betamethasone Dipropionate Cream USP, manufactured by Fougera Pharmaceuticals Inc. Betamethasone

Aurobindo Receives FDA Approval for Betamethasone Dipropionate Cream USP, 0.05% Read More »

Aurobindo Receives FDA Approval for Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, 2.5 mg/6.25 mg, 5 mg/6.25 mg, and 10 mg/6.25 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, 2.5 mg/6.25 mg, 5 mg/6.25 mg, and 10 mg/6.25 mg. Aurobindo Pharma’s Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, are an AB-rated generic equivalent to the reference

Aurobindo Receives FDA Approval for Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, 2.5 mg/6.25 mg, 5 mg/6.25 mg, and 10 mg/6.25 mg Read More »

Aurobindo Receives FDA Approval for Cariprazine Capsules, 1.5 mg, 3 mg, and 6 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Cariprazine Capsules, 1.5 mg, 3 mg, and 6 mg. Aurobindo Pharma’s Cariprazine Capsules are an AB-rated generic equivalent to the reference listed drug (RLD), Vraylar Capsules manufactured by AbbVie Inc. Cariprazine Capsules

Aurobindo Receives FDA Approval for Cariprazine Capsules, 1.5 mg, 3 mg, and 6 mg Read More »

Aurobindo Receives FDA Approval for Potassium Chloride Oral Solution USP, 10% (20 mEq/15 mL) and 20% (40 mEq/15 mL)

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Potassium Chloride Oral Solution USP, 10% (20 mEq/15 mL) and 20% (40 mEq/15 mL). Aurobindo Pharma’s Potassium Chloride Oral Solution USP, are an AB-rated generic equivalent to the reference listed drug (RLD),

Aurobindo Receives FDA Approval for Potassium Chloride Oral Solution USP, 10% (20 mEq/15 mL) and 20% (40 mEq/15 mL) Read More »

Aurobindo Receives FDA Approval for Fosfomycin Tromethamine Granules for Oral Solution, 3 grams

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Fosfomycin Tromethamine Granules for Oral Solution, 3 grams (Single-Dose Sachet). Aurobindo Pharma’s Fosfomycin Tromethamine Granules for Oral Solution, are an AB-rated generic equivalent to the reference listed drug (RLD), Monurol® Granules for

Aurobindo Receives FDA Approval for Fosfomycin Tromethamine Granules for Oral Solution, 3 grams Read More »

Aurobindo Receives FDA Approval for Linagliptin Tablets, 5 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Linagliptin Tablets, 5 mg. Aurobindo Pharma’s Linagliptin Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Tradjenta Tablets manufactured by Boehringer Ingelheim Pharmaceuticals, Inc. (Boehringer). Linagliptin Tablets are indicated

Aurobindo Receives FDA Approval for Linagliptin Tablets, 5 mg Read More »

Aurobindo Receives FDA Approval for Naproxen Oral Suspension USP, 125 mg/5 mL

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Naproxen Oral Suspension USP, 125 mg/5 mL. Aurobindo Pharma’s Naproxen Oral Suspension, are an AB-rated generic equivalent to the reference listed drug (RLD), Naprosyn Oral Suspension manufactured by Atnahs Pharma US Limited.

Aurobindo Receives FDA Approval for Naproxen Oral Suspension USP, 125 mg/5 mL Read More »

Aurobindo Receives FDA Approval for Prochlorperazine Maleate Tablets USP, 5 mg and 10 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Prochlorperazine Maleate Tablets USP, 5 mg and 10 mg. Aurobindo Pharma’s Prochlorperazine Maleate Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Compazine Tablets manufactured by GlaxoSmithKline (GSK) Prochlorperazine

Aurobindo Receives FDA Approval for Prochlorperazine Maleate Tablets USP, 5 mg and 10 mg Read More »

Aurobindo Receives FDA Approval for Deferasirox Oral Granules, 90 mg,180 mg, and 360 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Deferasirox Oral Granules, 90 mg,180 mg, and 360 mg. Aurobindo Pharma’s Deferasirox Oral Granules, are an AB-rated generic equivalent to the reference listed drug (RLD), Jadenu Sprinkle Granules manufactured by Novartis Pharmaceuticals

Aurobindo Receives FDA Approval for Deferasirox Oral Granules, 90 mg,180 mg, and 360 mg Read More »

Aurobindo Receives FDA Approval for Pirfenidone Tablets USP, 267 mg and 801 mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Pirfenidone Tablets USP, 267 mg and 801 mg. Aurobindo Pharma’s Pirfenidone Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Esbriet Tablets manufactured by Genentech Inc. (a subsidiary of

Aurobindo Receives FDA Approval for Pirfenidone Tablets USP, 267 mg and 801 mg Read More »

Aurobindo Receives FDA Approval for Lidocaine Hydrochloride Oral Topical Solution USP, 2%

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Lidocaine Hydrochloride Oral Topical Solution USP, 2%. Aurobindo Pharma’s Lidocaine Hydrochloride Oral Topical Solution, are an AB-rated generic equivalent to the reference listed drug (RLD), Xylocaine Oral Topical Solution manufactured by Fresenius

Aurobindo Receives FDA Approval for Lidocaine Hydrochloride Oral Topical Solution USP, 2% Read More »