14
Jan
Speed Limit 45 Radar Enforced road sign with passing cars on a California street.

The FDA’s Spotlight on CDER Science – Nitrosamines and the Acceptable Intake Approach

In the latest CDER Science Spotlights, available (here), the FDA provides some insight into the development of the Carcinogenic Potency Categorization Approach (CPCA) to determine recommended acceptable intake limits of N-nitrosamine impurities in drug products.  The latest revision of the Nitrosamine Impurity guidance updated in September 2024 (here) provided better integration of the overall assessment […]

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09
Jan
Focused businessman analyzing marketing reports on a desktop monitor and reviewing paper graphs, financial stats, and startup project infographics.

November 2024 Official OGD Statistics Published

The OGD published the second month of the Fiscal Year (FY) 2025 statistical report titled, Generic Drugs Program Monthly and Quarterly Activities Report (here).  There is some continued good news and also some troubling news in the report. On the positive side, we previously reported (here) in our unofficial posting, the full approval actions as […]

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06
Jan
Middle age senior hoary doctor man texting using smartphone over isolated background screaming proud and celebrating victory and success very excited, cheering emotion

December 2024 Brought Gifts for ANDA Approval Actions (Unofficially)

The OGD had some late-month stocking stuffers as it issued 68 full-approval actions and 16 tentative-approval actions for a total of 84 approval actions in December.  Despite the hectic holiday schedule, if these numbers are confirmed in the official totals for the month, it would mean that the OGD managed to tie the second highest […]

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30
Dec
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FDA Updates List of Off-Patent, Off-Exclusivity Drug Products With No Approved ANDAs

Twice a year, the FDA publishes an update of the List of Off‑Patent, Off‑Exclusivity Drugs without an Approved Generic (see the December 2024 listing here).  This list is designed to generate interest from the industry in increasing competition among such products and it is made up of two parts.  Part I is for drugs for which […]

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19
Dec
Generic Drug Cluster Has a Lot of Muster - Lachman Blog 2

Generic Drug Cluster Has a Lot of Muster!

The Generic Drug Cluster is a consortium of top regulatory agencies from around the world that get together to discuss common issues related to the drug approval process in an effort to better understand how each agency approaches various topics. Hopefully, these discussions will result in developing regulatory strategies that reflect the best and most […]

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17
Dec
December 2024 Unofficial Mid-Month ANDA Approval Actions - Lachman Blog

December 2024 Unofficial Mid-Month ANDA Approval Actions

As of December 15, 2024, just seven business days before Christmas, the OGD has issued 23 full-approval actions and 11 tentative-approval actions. With the holiday quickly approaching and facing what is likely a full FDA vacation schedule, what will the end of the month look like? A total of 34 full and tentative approval actions at […]

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09
Dec
OGD Official Statistics for First Month of FY 2025 Reported - Lachman Blog

OGD Official Statistics for First Month of FY 2025 Reported – ANDA Submissions Off to Slow Start

According to the first FY 2025 Generic Drugs Program Monthly and Quarterly Activities Report (here), the OGD had a good month for approval actions, issuing 62 full-approval actions and 20 tentative-approval actions for a total of 82. Only one month in FY 2024 had a higher combined total for these two metrics. That’s the good news! The […]

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02
Dec

Are You Handling USP Reference Standards Appropriately? 

Over 30 years ago, one of my responsibilities was overseeing the company’s Reference Standard Program for marketed products.  In-house standards were maintained and provided to company locations throughout the world, which also included providing enough fully characterized/qualified drug substances or impurities to the USP to be considered as a potential future USP Reference Standard lot.  […]

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26
Nov
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FDA Updates Warning for All NSAIDs; Other Drugs to Come?

For those of you who follow the daily approvals page (here), on November 21, 2024, there was a flurry of supplemental labeling approvals listed for drug products that contain non-steroidal anti-inflammatory drugs (NSAIDs), from aspirin to Zipsor (diclofenac potassium).  In today’s CDER Drug Safety-related Labeling Changes (SrLC), the new, revised warning that must be included was […]

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