4 results found containing all search terms.
Barr Laboratories announced a voluntary recall of 3 lots of its Nortrel 7/7/7 – 28 day (norethindrone and ethinyl estradiol tablets, USP) oral c...
... Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Nortrel 7 / 7 / 7-28 Day Oral Contraceptive (norethindrone and ethinyl estradiol tablets, USP) Audience: Pharmacists, reproductive health professionals, and consumers Barr Laboratories announced a voluntary recall of 3 lots of its Nortrel 7 / 7 / 7 â €“ 28 day (norethindrone and ethinyl estradiol tablets, USP) oral contraceptive product. The recall involves Lot Numbers 290122001, 290122002 and 290122003 and is being implemented because two individuals notified the company that the color-coded ... for Human Medical Products 2003 Safety Alerts for Human Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Nortrel 7 / 7 / 7-28 Day Oral Contraceptive (norethindrone and ethinyl estradiol tablets, USP) Audience: Pharmacists, reproductive health professionals, and consumers Barr Laboratories announced a voluntary recall of 3 lots of its Nortrel 7 / 7 / 7 â €“ 28 day (norethindrone and ethinyl estradiol tablets, USP) oral contraceptive product. The recall involves ...
URL: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm153330.htm
Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) Press Release Oct 2002
... for Human Medical Products-Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) Press Release Oct 2002 This is the text of a press release from Pharmacia. Contact the company for a copy of any referenced enclosures. PHARMACIA CORPORATION ANNOUNCES VOLUNTARY RECALL OF LUNELLE MONTHLY CONTRACEPTIVE INJECTION PEAPACK, N.J. (October 10, 2002)-Pharmacia Corporation announced today that the company is initiating a voluntary recall of Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) in prefilled syringes due to a lack of assurance ... for Human Medical Products 2004 Safety Alerts for Human Medical Products 2003 Safety Alerts for Human Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) Press Release Oct 2002 This is the text of a press release from Pharmacia. Contact the company for a copy of any referenced enclosures. PHARMACIA CORPORATION ANNOUNCES VOLUNTARY RECALL OF LUNELLE MONTHLY CONTRACEPTIVE INJECTION PEAPACK, N.J. (October 10, 2002)- ...
URL: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm170924.htm
Pharmacia announced a voluntary recall of all Lunelle prefilled syringe lots on the market, due to a lack of assurance of full potency and possibl...
... Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) Audience: Pharmacists and Reproductive healthcare professionals Pharmacia announced a voluntary recall of all Lunelle prefilled syringe lots on the market, due to a lack of assurance of full potency and possible risk of contraceptive failure. Lunelle packaged in vials is not affected by this recall. The affected lots were distributed in the United States, Puerto Rico and the ... for Human Medical Products 2004 Safety Alerts for Human Medical Products 2003 Safety Alerts for Human Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) Audience: Pharmacists and Reproductive healthcare professionals Pharmacia announced a voluntary recall of all Lunelle prefilled syringe lots on the market, due to a lack of assurance of full potency and possible risk of contraceptive failure. Lunelle packaged in vials is not affected by this ...
URL: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm154507.htm
2005 Safety Alerts for Human Medical Products
... 2005 Similac Advance with Iron powdered infant formula 02 / 16 / 2005 TMM brand Fortified Mineral Neutralizer and Ultra Fortified Mineral Neutralizer 05 / 20 / 2005-- Drugs and Therapeutic Biological Products (CDER) Product Name Date Issued / Updated Able Laboratories Products-Recall of all Manufactured Drugs 06 / 01 / 2005 Accutane and Isotretinoin 08 / 12 / 2005 Adderall XR (amphetamine) 02 / 10 / 2005 Advair Diskus (fluticasone propionate & salmeterol inhalation powder) 11 / 18 / 2005 Agrylin (anagrelide hydrochloride) 02 / 09 / ... 30, NovoLog insulin aspart (rDNA origin) injection 09 / 14 / 2005 NovoLog insulin aspart (rDNA origin) injection 09 / 14 / 2005 NeutroSpec (Technetium [99m Tc] fanolesomab) 12 / 02 / 2005 Ortho Evra (norelgestromin / ethinyl estradiol transdermal system) 11 / 14 / 2005 Palladone (hydromorphone hydrochloride) 07 / 14 / 2005 Paroxetine HCl-Paxil and generic paroxetine 12 / 08 / 2005 Paxil (paroxetine HCL ), Paxil CR Controlled-Release Tablets 09 / 27 / 2005 Paxil (paroxetine) 07 / 08 ...
URL: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm151239.htm
