Drug company (FDA labeler)
Medcore LLC
NDC labeler code: 82461
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
- Cyclobenzaprine hydrochlorideAmrix, Tonmya, Fexmid · 2 products
- MeloxicamZybic, Xifyrm, Qamzova · 2 products
- IbuprofenIbu, Caldolor · 2 products
- MethocarbamolRobaxin, Atmeksi, Tanlor · 2 products
- TizanidineZanaflex, Ontralfy · 2 products
- BaclofenGablofen, Lyvispah, Baclofen (Intrathecal) · 2 products
- LansoprazolePrevacid Solutab, Prevacid · 1 product
- LidocaineXylocaine Mpf, Xylocaine, Lidocaine Viscous · 1 product
- NaproxenNaprelan, Rugby All Day Relief · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| July 13, 2021 | ANDA214099 | Baclofen BACLOFEN | Aurobindo Pharma Ltd |
| April 30, 2021 | ANDA212623 | Methocarbamol METHOCARBAMOL | Pharmazone |
| April 30, 2020 | ANDA209190 | Lidocaine LIDOCAINE | Ibsa |
| February 21, 2020 | ANDA212517 | Naproxen NAPROXEN | Sciegen Pharms |
| January 18, 2019 | ANDA207394 | Lansoprazole LANSOPRAZOLE | Alkem Labs Ltd |
| May 31, 2017 | ANDA208170 | Cyclobenzaprine hydrochloride CYCLOBENZAPRINE HYDROCHLORIDE | Rubicon Research |
| November 23, 2016 | ANDA202413 | Ibuprofen IBUPROFEN | Shandong Xinhua |
| July 19, 2006 | ANDA077920 | Meloxicam MELOXICAM | Aiping Pharm Inc |
| September 29, 2003 | ANDA076416 | Tizanidine TIZANIDINE HYDROCHLORIDE | Sun Pharm Inds Inc |
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.
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