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Alpharma Receives USA FDA Tentative Approval for Lisinopril 20 mg, 30 mg and 40 mg Tablets.

Publication: PR Newswire
Publication Date: 12-MAR-02 		Format: Online - approximately 396 words
Delivery: Immediate Online Access

Article Excerpt
FORT LEE, N.J. -- Alpharma Inc. today announced that Purepac Pharmaceutical Co., a subsidiary of Alpharma, has received tentative approval from the United States Food and Drug Administration (FDA) to manufacture and market lisinopril 20 mg, 30 mg and 40 mg tablets. Final approval is pending the expiration of pediatric exclusivity on June 29, 2002.

Alpharma's lisinopril tablets,...

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