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FDA Daily

FDA daily for Monday, July 20, 2026

176 FDA records across 3 sections. 6 touch MedGrid's categories and are listed first.

176FDA Records
3 of 7Sections With Data
6Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Sun, Jul 19 (yesterday)
Nothing from FDA for this date
Drug approvalsCovers FDA's Mon, Jul 13 (a week ago)
1 touch MedGrid27
  • NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL AND FERROUS FUMARATETouches MedGrid categories

    ETHINYL ESTRADIOL, NORETHINDRONE ACETATE — XIROMED

    ANDA205049 · Labeling

  • ZITHROMAX

    AZITHROMYCIN — PFIZER

    NDA050670 · Labeling

  • CHILDREN'S ZYRTEC HIVES

    CETIRIZINE HYDROCHLORIDE — KENVUE BRANDS

    NDA022155 · Labeling

  • OXCARBAZEPINE

    OXCARBAZEPINE — PHARMAZONE

    ANDA217782 · Labeling

  • IRBESARTAN

    IRBESARTAN — CHARTWELL MOLECULAR

    ANDA077205 · Labeling

  • BRIVARACETAM

    BRIVARACETAM — SHANDONG

    ANDA219766 · Original approval

  • BUPRENORPHINE

    BUPRENORPHINE — WATSON LABS TEVA

    ANDA204937 · Labeling

  • ZITHROMAX

    AZITHROMYCIN — PFIZER

    NDA050711 · Labeling

  • ZITHROMAX

    AZITHROMYCIN — PFIZER

    NDA050710 · Labeling

  • ZITHROMAX

    AZITHROMYCIN — PFIZER

    NDA050730 · Labeling

  • ZITHROMAX

    AZITHROMYCIN — PFIZER

    NDA050733 · Labeling

  • LEQEMBI IQLIK

    LECANEMAB-IRMB — EISAI INC

    BLA761375 · Efficacy

Showing 12 of 27. Search the rest in openFDA.

Drug recallsCovers FDA's Mon, Jul 13 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Mon, Jul 13 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Mon, Jul 13 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Mon, Jul 6 (two weeks ago)
7
  • Cytrans™ Elashield

    GC America, Inc.

    K253317 · Substantially Equivalent · Dental

  • Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)

    SteriLance Medical (Suzhou), Inc.

    K260122 · Substantially Equivalent · General, Plastic Surgery

  • TESSA Spatial Surgery System; INTELLIO Tablet (72205455)

    Smith & Nephew, Inc.

    DEN250037 · Unknown · Orthopedic

  • Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit…

    Hartman Medical Group, LLC

    K261529 · Substantially Equivalent · Cardiovascular

  • MobileLink Acetabular Cup System – 40mm ID Inserts (various)

    Waldemar Link GmbH & Co. KG

    K261009 · Substantially Equivalent · Orthopedic

  • Plum Vagiceuticals™ Vaginal Moisturizing Suppositories

    PCCA, Inc.

    K261909 · Substantially Equivalent · Obstetrics/Gynecology

  • INDIRA CLOUD VIEWER

    INDIGO TECHNOLOGIES

    K261465 · Substantially Equivalent · Radiology

Label changesCovers FDA's Mon, Jul 6 (two weeks ago)
5 touch MedGrid142
  • Sunscreen SPF 50Touches MedGrid categories

    Worthy Promotional Products

    Label version 2

  • Estradiol valerateTouches MedGrid categories

    Xiromed, LLC

    Label version 10

  • Stay Ageless SunscreenTouches MedGrid categories

    TOXFAIRY, LLC

    Label version 1

  • Premier Tinted Mineral SunscreenTouches MedGrid categories

    Emerald Aesthetics LLC

    Label version 1

  • SPF 30 SunscreenTouches MedGrid categories

    Coconut Caliente Costa Rica LLC

    Label version 2

  • ENTRESTO

    Novartis Pharmaceuticals Corporation

    Label version 25

  • ropinirole

    Preferred Pharmaceuticals Inc.

    Label version 1

  • Rapidol Aspirin

    Pharmadel LLC

    Label version 6

  • Imipramine Hydrochloride

    REMEDYREPACK INC.

    Label version 8

  • Hand Sanitizing Wipes

    UpLift Brands LLC

    Label version 4

  • Lithium Carbonate

    REMEDYREPACK INC.

    Label version 15

  • Ezetimibe

    A-S Medication Solutions

    Label version 3

Showing 12 of 142. Search the rest in openFDA.

How the FDA Daily Is WrittenSources, dates and what gets flagged

Every issue is written from FDA's public data (openFDA) and nothing else: the counts, names, firms and reasons are FDA's own. openFDA posts each kind of record on its own delay, so each section covers one FDA date and says which. Shortages cover yesterday; approvals, drug recalls, device recalls and food and supplement recalls cover a week ago; device clearances and label changes cover two weeks ago. Every FDA date appears in exactly one issue. Items that touch the categories MedGrid works in, such as GLP-1s, hormones, injectables, peptides, compounded products and aesthetic devices, are marked and listed first.

Subscribe with any feed reader, or point an email tool at theRSS feed. For the rules behind the headlines, see Regulations Research.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.