Drug company (FDA labeler)
Dr. Reddy's Labratories Inc.
NDC labeler code: 75907
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
- ClonidineClonidine Transdermal System, Catapres-Tts-1, Clonidine Transdermal System Usp, 0.1 Mg/Day · 3 products
- DofetilideTikosyn · 3 products
- Liothyronine sodiumCytomel, Liomny · 3 products
- CyclophosphamideFrindovyx · 3 products
- DiltiazemTiadylt ER, Cartia Xt, Tiazac Extended Release · 3 products
- Disopyramide phosphateNorpace · 2 products
- NorethindroneErrin, Nora Be, Camila · 2 products
- Estazolam2 products
- Amiodarone hydrochloridePacerone, Nexterone · 2 products
- Tamoxifen citrateSoltamox · 2 products
- NystatinNystop, Klayesta, Nyamyc · 1 product
- FluorouracilFavlyxa, Tolak, Efudex · 1 product
- Butalbital and acetaminophenTencon, Allzital · 1 product
- Butalbital, acetaminophen and caffeineFioricet · 1 product
- Trimethoprim1 product
- ErythromycinEry, Ery-Tab · 1 product
- Brompheniramine maleate, pseudoephedrine hydrochloride, and dextromethorphan hydrobromide1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| May 5, 2022 | ANDA215775 | Diltiazem DILTIAZEM HYDROCHLORIDE | DR Reddys Labs SA |
| July 30, 2020 | NDA212501 | Cyclophosphamide CYCLOPHOSPHAMIDE | DR Reddys |
| December 4, 2018 | ANDA207676 | Brompheniramine maleate, pseudoephedrine hydrochloride, and dextromethorphan hydrobromide BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE | DR Reddys Labs SA |
| December 27, 2017 | ANDA207313 | Butalbital and acetaminophen BUTALBITAL AND ACETAMINOPHEN | DR Reddys Labs SA |
| June 6, 2016 | ANDA207058 | Dofetilide DOFETILIDE | DR Reddys Labs SA |
| August 20, 2010 | ANDA079090 | Clonidine CLONIDINE | DR Reddys Labs SA |
| March 20, 2009 | ANDA090097 | Liothyronine sodium LIOTHYRONINE SODIUM | DR Reddys Labs SA |
| April 11, 2008 | ANDA077524 | Fluorouracil FLUOROURACIL | DR Reddys Labs SA |
| July 15, 2004 | ANDA065203 | Nystatin NYSTATIN | DR Reddys Labs SA |
| February 20, 2003 | ANDA075797 | Tamoxifen citrate TAMOXIFEN CITRATE | DR Reddys Labs SA |
| October 21, 2002 | ANDA076177 | Norethindrone CAMILA | DR Reddys Labs SA |
| October 21, 2002 | ANDA076225 | Norethindrone ERRIN | DR Reddys Labs SA |
| January 25, 2001 | ANDA075389 | Amiodarone hydrochloride AMIODARONE HYDROCHLORIDE | DR Reddys Labs SA |
| July 10, 1997 | ANDA074921 | Estazolam ESTAZOLAM | DR Reddys Labs SA |
| March 17, 1986 | ANDA089007 | Butalbital, acetaminophen and caffeine BUTALBITAL, ACETAMINOPHEN AND CAFFEINE | DR Reddys Labs SA |
| May 31, 1985 | ANDA070173 | Disopyramide phosphate DISOPYRAMIDE PHOSPHATE | DR Reddys Labs SA |
| July 30, 1982 | NDA018679 | Trimethoprim TRIMETHOPRIM | DR Reddys Labs SA |
| January 26, 1981 | NDA050536 | Erythromycin ERYC | DR Reddys Labs SA |
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
- All drug companiesA to Z
- 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