Caraco Pharmaceutical Laboratories, Ltd. Announces Tentative FDA Approval For Generic Prandin(R)

Caraco Pharmaceutical
Laboratories, Ltd., (Amex: CPD) announced today that the US Food and Drug
Administration (FDA) has granted tentative approval for the Company's
Abbreviated New Drug Application (ANDA) for Repaglinide Tablets USP
(repaglinide), 0.5mg, 1mg and 2mg.



Repaglinide is indicated as an adjunct to diet and exercise to lower
the blood glucose in patients with type 2 diabetes mellitus (NIDDM) whose
hyperglycemia cannot be controlled satisfactorily by diet and exercise
alone. This tentative approval is the bioequivalent to Prandin(R), a
registered trademark of Novo Nordisk Pharmaceuticals, Inc. Prandin(R)
tablets had U.S. sales of approximately $153 million for the 12-month
period ended June 30, 2007, according to IMS Data.



Daniel H. Movens, Caraco's Chief Executive Officer, said, "We are
extremely pleased to receive this tentative approval. We believe we have a
first to file position on Repaglinide, which could result in 180-day
marketing exclusivity. The product was filed with a Paragraph IV
certification that we do not infringe and or that the Novo Nordisk patent
is invalid. We are under current litigation with Novo Nordisk and expect a
favorable conclusion."



Detroit-based Caraco Pharmaceutical Laboratories, Ltd., develops,
manufactures, markets and distributes generic and private-label
pharmaceuticals to the nation's largest wholesalers, distributors,
drugstore chains and managed care providers.



Safe Harbor: This news release contains forward-looking statements made
pursuant to the safe-harbor provisions of the Private Securities Litigation
Reform Act of 1995. Such statements are based on management's current
expectations and are subject to risks and uncertainties that could cause
actual results to differ materially from those described in the forward-
looking statements. These risks and uncertainties are contained in the
Corporation's filings with the Securities and Exchange Commission and
include, but are not limited to: information of a preliminary nature that
may be subject to adjustment, potentially not obtaining or delay in
obtaining FDA approval for new products, governmental restrictions on the
sale of certain products, development by competitors of new or superior
products or cheaper products or new technology for the production of
products, the entry into the market of new competitors, market and customer
acceptance and demand for new pharmaceutical products, availability of raw
materials, timing and success of product development and launches,
dependence on few products generating majority of sales, product liability
claims for which the Company may be inadequately insured, and other risks
identified in this report and from time to time in our periodic reports and
registration statements. These forward- looking statements represent our
judgment as of the date of this report. We disclaim, however, any intent or
obligation to update our forward-looking statements.


Caraco Pharmaceutical Laboratories, Ltd.

caraco

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