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American Pharmaceutical Partners receive FDA approval for ampicillin, sulbactam for injection
Schaumburg | Friday, December 2, 2005, 08:00 Hrs  [IST]

American Pharmaceutical Partners Inc. (APP) has received an approval from the US Food and Drug Administration for its abbreviated new drug application (ANDA) for the combination drug ampicillin and sulbactam for injection, USP, the generic equivalent of Pfizer Inc.'s Unasyn.

According to a company release, the annual sales in 2004 of this product exceeded $116 million, of which $83 million was sold in vials, according to IMS. APP expects to commence marketing ampicillin and sulbactam immediately.

"The addition of ampicillin and sulbactam brings to 17, the number of generic anti-infective products in our portfolio and bolsters our industry leading position for these types of injectable products. Our ability to provide customers with a wide array of anti-infectives enabled us to have GPO contracts in place at launch," said Patrick Soon-Shiong., chairman and chief executive officer.

Ampicillin and sulbactam will be available from APP in 1.5g and 3g single dose vials (SDV). The product is preservative-free and AP rated and each vial will include a bar code and latex-free vial stopper. The approval is the fifth product approval APP has received this year, adds the release.

Ampicillin and sulbactam is an injectable antibacterial combination consisting of the seminsynthetic antibiotic ampicillin sodium and the beta-lactamase inhibitor sulbactam sodium. Administered intravenously or intramuscular, Ampicillin and sulbactam is indicated for the treatment of several skin and skin structure, intra-abdominal and gynaecological infections due to susceptible strains of micro organisms.

American Pharmaceutical Partners Inc. is a specialty drug company that develops, manufactures and markets injectable pharmaceutical products, focusing on the oncology, anti-infective and critical care markets.

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