Drug company (FDA labeler)
LGM Pharma Solutions, LLC
Name in FDA records: LGM PHARMA SOLUTIONS, LLC
NDC labeler code: 79739
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- NabumetoneRelafen Ds · 3 products
- UrsodiolReltone 200 Mg, Ursolign, Urso Forte · 2 products
- Butalbital, aspirin, caffeine and codeine phosphateAscomp with Codeine · 1 product
- GlycopyrrolateGlyrx-Pf, Glycate, Cuvposa · 1 product
- Butalbital, aspirin, and caffeine1 product
- Butalbital, acetaminophen and caffeineFioricet · 1 product
- Butalbital, acetaminophen, caffeine and codeine phosphate1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| October 18, 2021 | ANDA205230 | Butalbital, aspirin, and caffeine BUTALBITAL, ASPIRIN AND CAFFEINE | Lgm Pharma |
| May 8, 2020 | ANDA205789 | Ursodiol URSODIOL | Lgm Pharma |
| August 30, 2019 | ANDA203166 | Nabumetone NABUMETONE | Lgm Pharma |
| October 31, 2018 | ANDA209587 | Butalbital, acetaminophen and caffeine BUTALBITAL, ACETAMINOPHEN AND CAFFEINE | Lgm Pharma |
| March 12, 2012 | ANDA091522 | Glycopyrrolate GLYCOPYRROLATE | Lgm Pharma |
| June 10, 2004 | ANDA076560 | Butalbital, acetaminophen, caffeine and codeine phosphate BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE | Lgm Pharma |
| November 30, 2001 | ANDA075231 | Butalbital, aspirin, caffeine and codeine phosphate BUTALBITAL, ASPIRIN, CAFFEINE, AND CODEINE PHOSPHATE | Lgm Pharma |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
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Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026