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    NEWS

    DRUGS & DEVELOPMENTS

    MARKET INTEL by PharmaCompass

    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.
    All News #Library
    Quality

    Long-standing issues result in warning letter for Teva

    IN-PHARMATECHNOLOGIST

    EU Regulatory Roundup: UK NHS Calls for Changes to Pricing Legislation

    RAPS

    Irbesartan blood pressure and heart medication recalled from pharmacies by MHRA

    GOV UK

    Valsartan products under recall - Updated October 24, 2018

    FDA

    Teva recalls 500,000 units of diabetes drug manufactured by Patheon

    FIERCE PHARMA

    Endo`s Par recalls half a million birth control pills made by Patheon

    FIERCE PHARMA

    Allergan recalls some Tazorac acne gel

    FIERCE PHRAMA

    Actavis recalls pills made by Patheon

    FIERCE MANUFACTURING

    FTC Issues Report on ANDA Settlement Agreements

    PATENT DOCS

    FDA cautions about dose confusion and medication error with Avycaz

    FDA

    King Drug Co. of Florence, Inc. v. SmithKline Beecham Corp. (3rd Cir. 2015)

    PATENT DOCS

    G.D. Searle LLC v. Lupin Pharmaceuticals, Inc. (Fed. Cir. 2015)

    PATENT DOCS

    FDA asks dermal filler makers to indicate risk of serious injury

    REUTERS

    Another Punt Return Resolving 180-Day Exclusivity; This Time a True Post-MMA Case Made in the Context of Lamotrigine Orally Disintegrating Tablets

    FDA LAW BLOG

    Actavis Laboratories, Ongoing Class III recall of Flurandrenolide Tape, USP, 4 mcg per sq cm, Rx Only. Distributed By: Actavis Pharma, Inc., Parsippany, NJ 07054, Manufactured By: 3M Company, St. Paul, MN, 55144. Labeled as A) Cordran Tape, Small Rolls, 24 in x 3 in, NDC: 52544-044-24, B) Cordran Tape, Large Rolls, 80 in x 3 in, NDC: 52544-044-80, C) Haelan Tape (Fludroxycortide), Bulk Rolls, NDC: 55515-014-00. because of Subpotent Drug: Flurandrenolide is subpotent.

    FDA

    Actavis Laboratories, FL, Inc., Ongoing Class III recall of Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90 because of Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell

    FDA

    Parents sue Botox maker after woman with cerebral palsy dies

    YAHOO FINANCE

    Allergan Drops Valeant-Ackman Insider Trading Lawsuit

    FIERCE PHARMA

    Actavis Inc, Ongoing Class II recall of Vancomycin Hydrochloride Capsules, USP, 125 mg, 250 mg, 2 x 10 count blister pack, Rx Only, Manufactured for Watson Pharma Inc., Parsippany, NJ 07054, by Patheon Pharmaceuticals Inc., Cincinnati, OH. NDC 0591-3560-15, NDC 0591-3561-15 because of Subpotent: Vancomycin 125 mg and 250mg capsules are being recalled due to subpotency.

    FDA

    Actavis Elizabeth LLC, Ongoing Class II recall of Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, 90-count bottles, Rx Only, Manufactured by: Actavis Elizabeth LLC, Elizabeth, NJ 07201 USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA; NDC 45963-305-09, UPC 3 45963-305-09 1. because of Failed Dissolution Specifications

    FDA

    Horizon Pharma Plc Files Patent Infringement Lawsuit Against Watson Laboratories, Inc. for Filing an ANDA Against PENNSAID(R) 2%

    HORIZON PHARMA

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