Drug company (FDA labeler)
TAGI Pharma, Inc.
NDC labeler code: 51224
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
- Benzonatate2 products
- Metformin hydrochlorideGlumetza · 2 products
- ChlorthalidoneThalitone, Hemiclor · 2 products
- CholestyramineQuestran, Prevalite, Cholestyramine Light · 2 products
- GabapentinNeurontin, Gralise, Relgaabi · 2 products
- AzithromycinZithromax, Azasite · 2 products
- LevetiracetamKeppra, Spritam, Keppra XR · 1 product
- Phentermine hydrochlorideLomaira · 1 product
- Naltrexone hydrochloride1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| February 24, 2022 | ANDA212875 | Chlorthalidone CHLORTHALIDONE | Pharmobedient |
| February 24, 2022 | ANDA212878 | Chlorthalidone CHLORTHALIDONE | Pharmobedient |
| March 9, 2021 | ANDA209597 | Cholestyramine CHOLESTYRAMINE | Pharmobedient |
| November 12, 2020 | ANDA209599 | Cholestyramine CHOLESTYRAMINE LIGHT | Pharmobedient Cnsltg |
| April 17, 2019 | ANDA208250 | Azithromycin AZITHROMYCIN | Cspc Ouyi |
| October 25, 2018 | ANDA208249 | Azithromycin AZITHROMYCIN | Cspc Ouyi |
| March 20, 2018 | ANDA209781 | Levetiracetam LEVETIRACETAM | Hainan Poly Pharm |
| October 26, 2017 | ANDA207057 | Gabapentin GABAPENTIN | Cspc Ouyi |
| July 31, 2015 | ANDA202765 | Benzonatate BENZONATATE | Cspc-Nbp Pharm |
| January 31, 2011 | ANDA200272 | Phentermine hydrochloride PHENTERMINE HYDROCHLORIDE | Elite Labs |
| April 17, 2008 | ANDA078321 | Metformin hydrochloride METFORMIN HYDROCHLORIDE | Cspc Ouyi |
| May 26, 1999 | ANDA075274 | Naltrexone hydrochloride NALTREXONE HYDROCHLORIDE | Elite Labs |
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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- All prescription drugs A to ZSearch by generic, brand or Spanish name
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