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TARO
FDA Approves Unknown Drug — TARO

# FDA Approves TARO's Generic Drug Application Taro Pharmaceutical Industries has received FDA approval for ANDA 079204, expanding its generic drug p...

SANDOZ
FDA Approves Unknown Drug — SANDOZ

# FDA Approves Sandoz Generic Drug Application Sandoz received FDA approval for ANDA040719 on January 29, 2009, expanding its generic drug portfolio ...

Mylan
FDA Approves DIVALPROEX SODIUM — Mylan Pharmaceuticals Inc.

Mylan Pharmaceuticals Inc. secured FDA approval for its generic Divalproex Sodium, a substance used to treat epilepsy and bipolar disorder, positionin...

RISING
FDA Approves Unknown Drug — RISING

# FDA Approves Rising's Generic Drug Application Rising Pharmaceuticals received FDA approval for its abbreviated new drug application (ANDA077420) o...

Aurobindo
FDA Approves LAMOTRIGINE — Aurobindo Pharma Limited

Aurobindo Pharma Limited secured final FDA approval for its generic Lamotrigine oral tablets, a development anticipated to enhance the company's marke...

Advagen
FDA Approves LAMOTRIGINE — Advagen Pharma Limited

Advagen Pharma Limited announced the FDA approval of its generic oral LAMOTRIGINE formulation under ANDA078625, granting the company immediate access ...

Sun
FDA Approves LAMOTRIGINE — Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc. announced that the FDA approved its Abbreviated New Drug Application (ANDA078525) for oral lamotrigine, enabling t...

OWP
FDA Approves LAMOTRIGINE KIT — OWP Pharmaceuticals, Inc.

OWP Pharmaceuticals, Inc. received FDA approval for its multi-strength Lamotrigine oral kit, marking its entry into the antiepileptic market and enabl...

PHARMOBEDIENT
FDA Approves Unknown Drug — PHARMOBEDIENT

# FDA Approves PHARMOBEDIENT ANDA Application PHARMOBEDIENT has received FDA approval for ANDA078190, marking the company's entry into an additional ...

SUN
FDA Approves Unknown Drug — SUN PHARM INDS INC

Sun Pharma Industries Inc. announced FDA approval for its Isosorbide Mononitrate Extended-Release Tablets, expanding the generic giant's portfolio and...

INDICUS
FDA Approves Unknown Drug — INDICUS PHARMA

Indicator Pharma has secured FDA approval for its generic drug application, marking a potential commercial victory pending further specification of th...

Sandoz
FDA Approves MYCOPHENOLATE MOFETIL — Sandoz Inc

Sandoz Inc. has received FDA approval for Mycophenolate Mofetil (ANDA065379) in the oral tablet dosage form, sparking concerns regarding potential rev...

Sandoz
FDA Approves MYCOPHENOLATE MOFETIL — Sandoz Inc

Sandoz Inc received FDA approval for its generic version of mycophenolate mofetil on October 15, 2008. This approval marked a significant milestone in...

RISING
FDA Approves Unknown Drug — RISING

**WEGO Pharms** has received final approval from the FDA for its Abbreviated New Drug Application #ANDA077858, a pivotal move that positions the compa...

APOTEX
FDA Approves Unknown Drug — APOTEX

# FDA Approves Apotex Generic Drug Application Apotex Inc. received FDA approval for an abbreviated new drug application (ANDA077982) on August 4, 20...

APOTEX
FDA Approves Unknown Drug — APOTEX

Apotex's FDA approval for ANDA 077615 on July 29 signals a strategic push to capitalize on market competition, positioning the company to capture sign...

Hikma
FDA Approves MYCOPHENOLATE MOFETIL — Hikma Pharmaceuticals USA Inc.

Eleven years after approval, Hikma Pharmaceuticals had successfully transitioned to the first-to-file ANDA for mycophenolate mofetil, achieving signif...

HIKMA
FDA Approves Unknown Drug — HIKMA

Based on the provided incomplete data, a realistic financial newswire statement would be: HIKMA announced today that it received FDA approval for its...

Bayer
FDA Approves EOVIST — Bayer HealthCare Pharmaceuticals Inc.

# FDA Approves Bayer's EOVIST for Hepatic Imaging The U.S. Food and Drug Administration has approved Bayer HealthCare Pharmaceuticals' EOVIST (gadoxe...

HERITAGE
FDA Approves Unknown Drug — HERITAGE PHARMA AVET

Heritage Pharma Avet has secured FDA approval for its Abbreviated New Drug Application (ANDA 076228), a development expected to generate new revenue s...