Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. This recall was prompted due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) a possible process impurity or contaminant in an active pharmaceutical ingredient, manufactured by Hetero Labs Limited, Unit – I (API manufacturer).
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Thursday, February 28, 2019
Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 25 mg, 50 mg and 100 mg Due to the Detection of Trace Amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) Impurity found in the Active Pharmaceutical Ingredient (API) - FDA Safety Alerts & Drug Recalls
FDA warns CanaRx for selling unapproved, misbranded and unsafe imported drugs to unsuspecting Americans - FDA Press Releases
FDA issued a warning letter to CanaRx for illegally distributing drugs into the U.S. that have not been approved by the FDA for safety and effectiveness.
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Albumycin, a new isoindolequinone from Streptomyces albus J1074 harboring the fluostatin biosynthetic gene cluster - Journal of Antibiotics
Albumycin, a new isoindolequinone from Streptomyces albus J1074 harboring the fluostatin biosynthetic gene cluster
Albumycin, a new isoindolequinone from <i>Streptomyces albus</i> J1074 harboring the fluostatin biosynthetic gene cluster, Published online: 28 February 2019; doi:10.1038/s41429-019-0161-4
Albumycin, a new isoindolequinone from Streptomyces albus J1074 harboring the fluostatin biosynthetic gene clusterfrom The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2BYzukr
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Glycosylation of an allenic erythronolide - Journal of Antibiotics
Glycosylation of an allenic erythronolide
Glycosylation of an allenic erythronolide, Published online: 28 February 2019; doi:10.1038/s41429-019-0156-1
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Wednesday, February 27, 2019
Joy Gourmet Foods LLC Issues Allergy Alert on Undeclared Sulfites - FDA Safety Alerts & Drug Recalls
Joy Gourmet Foods Inc. of Maspeth, NY is recalling its Joy Brand Chutneys and Pastes products because they contain undeclared sulfites.. People who have allergies to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product. The recalled Joy Brand Chutneys and Pastes were distributed in NY, NJ,and CT in retail stores.The products comes in 8 oz,14 oz,16 oz, and 26 oz, 32 oz. clear glass jar packages and marked on the labels as follows:
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Statement from FDA Commissioner Scott Gottlieb, M.D. as prepared for oral testimony before the U.S. House Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies, Committee on Appropriations - FDA Press Releases
FDA addresses the U.S. House Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies, Committee on Appropriations
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Tuesday, February 26, 2019
UTZ Quality Foods Issues Allergy Alert on Undeclared Milk in Bachman 10 Ounce Twist - FDA Safety Alerts & Drug Recalls
Utz Quality Foods, LLC., is voluntarily recalling a specific expiration date code of Bachman 10 oz Twist Pretzel packages due to undeclared milk. This recall was initiated after reviewing production records which identified a small number of packages were mislabeled.
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