Generic Dilatrate-SR Availability
Dilatrate-SR is a brand name of isosorbide dinitrate, approved by the FDA in the following formulation(s):
DILATRATE-SR (isosorbide dinitrate - capsule, extended release; oral)
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Manufacturer: SCHWARZ PHARMA
Approval date: September 2, 1988
Strength(s): 40MG [RLD]
Has a generic version of Dilatrate-SR been approved?
No. There is currently no therapeutically equivalent version of Dilatrate-SR available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Dilatrate-SR. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Related Patents
There are no current U.S. patents associated with Dilatrate-SR.
See also...
- Dilatrate-SR Consumer Information (Wolters Kluwer)
- Dilatrate-SR Consumer Information (Cerner Multum)
- Dilatrate-SR Advanced Consumer Information (Micromedex)
- Isosorbide dinitrate Consumer Information (Wolters Kluwer)
- Isosorbide dinitrate extended-release Consumer Information (Wolters Kluwer)
- Isosorbide dinitrate Consumer Information (Cerner Multum)
- Apo-Isdn Advanced Consumer Information (Micromedex)
- Isosorbide dinitrate Oral, Sublingual Advanced Consumer Information (Micromedex)
Glossary
| Term | Definition |
|---|---|
| Drug Patent | A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation. |
| Drug Exclusivity | Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. |
| RLD | A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. |
