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Drugs@FDA: FDA-Approved Drugs

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Original NDA and Original BLA Approvals
July 2017

This report includes NDAs [including NDAs for new molecular entities (NMEs)] and BLAs (including new biological products) approved for the first time during the selected month. Original BLA/NDA approvals by CBER are not included in Drugs@FDA. This report does not include approved NDA or BLA supplements, approved ANDAs, or tentatively approved ANDAs/NDAs.

Click on the Drug Name and Application Number to see information about the drug (for example, regulatory history, labeling, reviews by FDA staff).

This report was produced on September 18, 2024.

Approval Date Drug Name Active Ingredients Submission Classification * Review Priority ** Company
07/05/2017 OMEPRAZOLE
NDA #209400
OMEPRAZOLE Type 3 - New Dosage Form Standard DEXCEL
07/07/2017 ENDARI
NDA #208587
L-GLUTAMINE Type 5 - New Formulation or New Manufacturer Standard EMMAUS MEDCL
07/13/2017 TREMFYA
BLA #761061
GUSELKUMAB JANSSEN BIOTECH
07/14/2017 ZYPITAMAG
NDA #208379
PITAVASTATIN MAGNESIUM Type 2 - New Active Ingredient Standard MEDICURE
07/17/2017 NERLYNX
NDA #208051
NERATINIB MALEATE Type 1 - New Molecular Entity Standard PUMA BIOTECH
07/18/2017 VOSEVI
NDA #209195
SOFOSBUVIR; VELPATASVIR; VOXILAPREVIR Type 1 - New Molecular Entity and Type 4 - New Combination Priority GILEAD SCIENCES INC
07/20/2017 BENLYSTA
BLA #761043
BELIMUMAB GLAXOSMITHKLINE LLC
07/26/2017 NITYR
NDA #209449
NITISINONE Type 5 - New Formulation or New Manufacturer Standard CYCLE
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