Authorized Generics and ANDA Products
GREENSTONE generic medications cover a broad range of therapeutic areas. Our authorized generics contain the same active1 and inactive ingredients in the same concentration and dosage strengths as their branded equivalents. View the table below for information about GREENSTONE’s portfolio of generic medicines.
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Noted products are trademarks or registered trademarks of their respective owners.
The Product Fact Sheet information provided is subject to change without notice. GREENSTONE is not responsible for systems and databases external to GREENSTONE that may use this information in its current form or as superseded by future changes.
GREENSTONE develops a Material Safety Data Sheet (MSDS) for each of its products to help its customers' occupational health and safety specialists assure workplace safety and comply with applicable laws. MSDSs are not intended to be used by GREENSTONE's patients as a replacement for, or as a complement to, Prescribing Information (such as package inserts) or the advice of a healthcare professional.
The MSDSs provided on this Web site were developed in good faith and believed accurate. Once a MSDS is printed out, it can no longer be updated by electronic means and may be superseded by updated online versions that contain materially different information. Therefore, the user is cautioned that the hard copy may become obsolete over time.
Access to GREENSTONE's MSDSs is provided ONLY for noncommercial use, provided that all copyright or other proprietary notices or disclaimers are retained.
GREENSTONE's MSDSs are furnished AS IS WITHOUT WARRANTY OF ANY KIND, WHETHER EXPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE. GREENSTONE assumes no liability of any kind that arises from your use of any of the MSDSs obtained through this site.
References: 1. US Food and Drug Administration.
Generic drugs: questions and answers. Drugs. September 3, 2013.
http://www.fda.gov/Drugs/ResourcesForYou/Consumers/QuestionsAnswers/ucm100100.htm. Accessed March 24, 2014.
You are encouraged to report negative side effects of prescription drugs to the
Visit www.fda.gov/medwatch or call 1-800-FDA-1088.