Aurobindo Receives FDA Approval for Colchicine Capsules, 0.6 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 Colchicine Capsules, 0.6 mg. Aurobindo Pharma’s Colchicine Capsules, are an AB-rated generic equivalent to the reference listed drug (RLD),Mitigare Capsules manufactured by Hikma International Pharmaceuticals LLC. Colchicine Capsules are indicated for: Prophylaxis […]

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Aurobindo Receives FDA Approval for Haloperidol Tablets USP, 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg and 20 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 Haloperidol Tablets USP, 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg and 20 mg. Aurobindo Pharma’s Haloperidol Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Haldol®

Aurobindo Receives FDA Approval for Haloperidol Tablets USP, 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg and 20 mg Read More »

Aurobindo Receives FDA Approval for Betamethasone Dipropionate Ointment USP, (Augmented), 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 Ointment USP, (Augmented), 0.05%. Aurobindo Pharma’s Betamethasone Dipropionate Ointment, are an AB-rated generic equivalent to the reference listed drug (RLD), Diprolene® Ointment manufactured by Organon LLC. Betamethasone Dipropionate Ointment are

Aurobindo Receives FDA Approval for Betamethasone Dipropionate Ointment USP, (Augmented), 0.05% Read More »

Aurobindo Receives FDA Approval for Desmopressin Acetate Tablets, 0.1 mg and 0.2 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 Desmopressin Acetate Tablets, 0.1 mg and 0.2 mg. Aurobindo Pharma’s Desmopressin Acetate Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), DDAVP Tablets manufactured by Ferring Pharmaceuticals, Inc. Desmopressin

Aurobindo Receives FDA Approval for Desmopressin Acetate Tablets, 0.1 mg and 0.2 mg Read More »

Aurobindo Receives FDA Approval for Mometasone Furoate Monohydrate Nasal Spray, 50 mcg/spray

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Mometasone Furoate Monohydrate Nasal Spray, 50 mcg/spray. Aurobindo Pharma’s Mometasone Furoate Monohydrate Nasal Spray, are an AB-rated generic equivalent to the reference listed drug (RLD), Nasonex Nasal Spray manufactured by Organon LLC.

Aurobindo Receives FDA Approval for Mometasone Furoate Monohydrate Nasal Spray, 50 mcg/spray Read More »

Aurobindo Receives FDA Approval for Fingolimod Capsules, 0.5 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 Fingolimod Capsules, 0.5 mg. Aurobindo Pharma’s Fingolimod Capsules, are an AB-rated generic equivalent to the reference listed drug (RLD), Gilenya Capsules manufactured by Novartis Pharmaceuticals Corporation. Fingolimod Capsules are indicated for: The

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Aurobindo Receives FDA Approval for Mycophenolic Acid Delayed-Release Tablets USP, 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 Mycophenolic Acid Delayed-Release Tablets USP, 180 mg and 360 mg. Aurobindo Pharma’s Mycophenolic Acid Delayed-Release Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Myfortic Delayed-Release Tablets manufactured by

Aurobindo Receives FDA Approval for Mycophenolic Acid Delayed-Release Tablets USP, 180 mg and 360 mg Read More »

Aurobindo Receives FDA Approval for Mycophenolate Mofetil Tablets USP, 500 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 Mycophenolate Mofetil Tablets USP, 500 mg. Aurobindo Pharma’s Mycophenolate Mofetil Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), Cellcept Tablets manufactured by Roche Palo Alto LLC. Mycophenolate Mofetil

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Aurobindo Receives FDA Approval for Atorvastatin Calcium Tablets USP, 10 mg, 20 mg, 40 mg, and 80 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 Atorvastatin Calcium Tablets USP, 10 mg, 20 mg, 40 mg, and 80 mg. Aurobindo Pharma’s Atorvastatin Calcium Tablets, are an AB-rated generic equivalent to the reference listed drug (RLD), LIPITOR® Tablets manufactured

Aurobindo Receives FDA Approval for Atorvastatin Calcium Tablets USP, 10 mg, 20 mg, 40 mg, and 80 mg Read More »

Aurobindo Receives FDA Approval for Deflazacort Tablets 6mg, 18mg, 30mg, & 36mg

East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Deflazacort Tablets, 6mg, 18mg, 30mg, & 36mg. Aurobindo Pharma’s Deflazacort Tablets are an AB-rated generic equivalent to the reference listed drug (RLD), EMFLAZA® Tablets manufactured by PTC Therapeutics Inc.  Deflazacort Tablets are

Aurobindo Receives FDA Approval for Deflazacort Tablets 6mg, 18mg, 30mg, & 36mg Read More »

Aurobindo Receives FDA Approval for Isotretinoin Capsules USP, 10 mg, 20 mg, 25 mg, 30 mg, 35 mg, and 40 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 Isotretinoin Capsules USP, 10 mg, 20 mg, 25 mg, 30 mg, 35 mg, and 40 mg. Aurobindo Pharma’s Isotretinoin Capsules, are an AB-rated generic equivalent to the reference listed drug (RLD), Absorica®

Aurobindo Receives FDA Approval for Isotretinoin Capsules USP, 10 mg, 20 mg, 25 mg, 30 mg, 35 mg, and 40 mg Read More »

Aurobindo Receives FDA Approval for Lacosamide Oral Solution USP, 10 mg/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 Lacosamide Oral Solution USP, 10 mg/mL. Aurobindo Pharma’s Lacosamide Oral Solution, are an AB-rated generic equivalent to the reference listed drug (RLD), VIMPAT® Oral Solution manufactured by UCB, Inc. Lacosamide Oral Solution

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