BNET Industries
Last Fiscal Year Sales:$103.1M
- Public
- US
Dow Jones Description
Able Laboratories, Inc. was a developer and manufacturer of generic pharmaceutical products in tablet, capsule, liquid and suppository dosage forms. In May 2005, Able suspended manufacturing and distribution of its entire product line. The company currently is not generating income or revenue, because of its suspension of manufacturing operations and product recalls. The company has filed a petition to reorganize under Chapter 11 of the United States Bankruptcy Code in the United States Bankruptcy Court for the District of New Jersey, Trenton Division on July 18, 2005.
Vice President, Compliance & Regulatory Affairs
Iva KlemickNumber of Employees 421
Peer Companies
NAICS Code Pharmaceutical Preparation Manufacturing: 325412
News & Analysis
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able laboratories inc. - All News and Analysis
Able Laboratories Announces Approval of Listing Application for Nasdaq National Market
Business Editors/Health/Medical Writers SOUTH PLAINFIELD, N.J.--BUSINESS WIRE--Feb. 26, 2003 Nasdaq National Market Trading Expected to Begin Thursday, February 27, 2003 Under the Existing Symbol "ABRX" Able Laboratories, Inc. (Nasdaq:ABRX) (BSE:AAB), today announced that the Nasdaq National Market has approved its application to list its common stock...
Able Laboratories Announces Approval of Listing Application for Nasdaq SmallCap Market
Business Editors & Health/Medical Writers SOUTH PLAINFIELD, N.J.--BUSINESS WIRE--Nov. 14, 2002 Nasdaq Trading Expected to Begin Tuesday, November 19, 2002 under Symbol ``ABRX'' Able Laboratories, Inc. (OTCBB:ABLA) today announced that the Nasdaq Stock Market has approved Able's application to list its common stock on the Nasdaq...
Able Laboratories, Inc. Corrects Contact Phone Number for Catherine M. Frost; 978/282-0065 Sted 908/754-2253 x529
Business Editors/Health & Medical Writers CORRECTION...by Able Laboratories, Inc. --BUSINESS WIRE In BW2252, (NJ-ABLE-LABORATORIES) Receives FDA Approval for the Generic Version of Esgic Plus Tablets, at the end of the release, contact phone number for Catherine M. Frost should read xxx 978/282-0065 (sted 908/754-2253 x529).
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Decision Makers
| Name (plus bio) | Position |
|---|---|
| Iva Klemick | Vice President, Compliance & Regulatory Affairs |
Iva Klemick as Vice President, Compliance & Regulatory Affairs, joined the Company in 1999 bringing over 25 years of experience in all areas of pharmaceutical operations including manufacturing, materials management, quality assurance, quality control and regulatory affairs. Prior to joining Able, she held Corporate Director positions in Planning, Material Management and QA/QC at Zenith Laboratories for over eight years. In her current position as Vice President, Compliance, Ms. Klemick is responsible for the management of ANDA filings and communications with all regulatory agencies.
| Organization | Position | Status |
|---|---|---|
| Able Laboratories, Inc. | Vice President, Compliance & Regulatory Affairs | Current |
| Able Laboratories, Inc. | Director, Regulatory Affairs | Former |
| Able, LLC | Former |
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