Genentech Inc

FDA Drug Class II Terminated

Cathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA 94080, NDC 50242-041-64

May 20, 2024 Genentech Inc Lot:3618858 = 105,759; Lot:3618873 =90,359 units

FDA Drug Class III Terminated

Susvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susvimo single-dose vial and One Susvimo initial fill needle, NDC 50242-078-55; and b) carton labeled as Susvimo Oc

October 18, 2022 Genentech Inc 452 vials and implants units

FDA Drug Class II Terminated

Xolair (omalizumab) Injection, 150 mg/1 mL, 1 prefilled syringe, Rx Only, For Subcutaneous Use. Single-Dose Prefilled Syringe. Product of France, Manufactured by: Genentech, Inc. A Member of the Roche

June 9, 2021 Genentech Inc 88,620 prefilled syringes units

FDA Drug Class III Terminated

Evrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after constitution, Rx only, Distributed by: Genentech, Inc. NDC:50242-175-05

April 20, 2021 Genentech Inc 2,627 bottles units

FDA Drug Class III Terminated

Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0

February 5, 2018 Genentech Inc 3,192 bottles units

FDA Drug Class I Terminated

Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device. Manufactured by: Genentech, Inc. 1 D

September 5, 2017 Genentech Inc 16,882 units

FDA Drug Class II Terminated

Cotellic (cobimetinib) Tablets, 20 mg, 63 count bottle, Rx Only, Made in Switzerland. Distributed by Genentech USA, Inc., South Francisco, CA. 94080, NDC 50242-717-01,UPC 3 50242-717-01.

March 13, 2017 Genentech Inc 748 bottles units

FDA Drug Class III Terminated

CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed

September 27, 2012 Genentech Inc 1128 bottles units

FDA Drug Class II Terminated

Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL Genentech, South San Francisco, CA 94080, NDC#50242-0076-01

September 20, 2012 Genentech Inc 10,306 syringes units

FDA Drug Class II Terminated

Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL Genentech, South San Francisco, CA 94080, NDC#50242-0074-01

September 20, 2012 Genentech Inc 12,791 syringes units

FDA Drug Class I Terminated

Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg); 1 20 mL multiple dose vial Bacteriostatic Water for Injection, USP (1.1% benzyl alcohol), Manufactured by Hospira, Inc., for Ge

July 30, 2012 Genentech Inc 2,140 kits units