Drug company (FDA labeler)
Dr.Reddy's Laboratories Ltd.
NDC labeler code: 55111
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
- OlanzapineZyprexa, Zyprexa Zydis, Olanzapine Intramuscular · 3 products
- Venlafaxine hydrochlorideEffexor XR · 3 products
- Divalproex sodiumDepakote, Depakote ER, Depakote Sprinkles · 3 products
- LansoprazolePrevacid Solutab, Prevacid · 2 products
- Zoledronic acidReclast · 1 product
- Levocetirizine dihydrochlorideXyzal · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| March 29, 2013 | ANDA091363 | Zoledronic acid ZOLEDRONIC ACID | DR Reddys Labs Ltd |
| April 23, 2012 | ANDA076255 | Olanzapine OLANZAPINE | DR Reddys Labs Ltd |
| March 15, 2012 | ANDA090161 | Divalproex sodium DIVALPROEX SODIUM | DR Reddys Labs Ltd |
| March 12, 2012 | ANDA090070 | Divalproex sodium DIVALPROEX SODIUM | Reddys |
| October 24, 2011 | ANDA076133 | Olanzapine OLANZAPINE | DR Reddys Labs Ltd |
| May 6, 2011 | ANDA078421 | Venlafaxine hydrochloride VENLAFAXINE HYDROCHLORIDE | DR Reddys Labs Ltd |
| February 24, 2011 | ANDA090392 | Levocetirizine dihydrochloride LEVOCETIRIZINE DIHYDROCHLORIDE | DR Reddys Labs Ltd |
| October 15, 2010 | ANDA091269 | Lansoprazole LANSOPRAZOLE | DR Reddys Labs Ltd |
| January 23, 2009 | ANDA078979 | Divalproex sodium DIVALPROEX SODIUM | DR Reddys Labs Ltd |
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