Generic Fragmin Availability
Last updated on Jun 11, 2025.
Fragmin is a brand name of dalteparin, approved by the FDA in the following formulation(s):
FRAGMIN (dalteparin sodium - injectable;injection)
-
Manufacturer: PFIZER
Approval date: April 4, 2002
Strength(s): 7,500 IU/0.75ML (discontinued)
FRAGMIN (dalteparin sodium - injectable;subcutaneous)
-
Manufacturer: PFIZER
Approval date: December 22, 1994
Strength(s): 2,500IU/0.2ML (12,500IU/ML) [RLD] -
Manufacturer: PFIZER
Approval date: March 18, 1996
Strength(s): 5,000IU/0.2ML (25,000IU/ML) [RLD] -
Manufacturer: PFIZER
Approval date: January 30, 1998
Strength(s): 10,000IU/ML (10,000IU/ML) [RLD] -
Manufacturer: PFIZER
Approval date: April 4, 2002
Strength(s): 7,500IU/0.3ML (25,000IU/ML) [RLD], 95,000IU/3.8ML (25,000IU/ML) [RLD], 95,000IU/9.5ML (10,000IU/ML) (discontinued) -
Manufacturer: PFIZER
Approval date: May 1, 2007
Strength(s): 10,000IU/0.4ML (25,000IU/ML) (discontinued), 12,500IU/0.5ML (25,000IU/ML) [RLD], 15,000IU/0.6ML (25,000IU/ML) [RLD], 18,000IU/0.72ML (25,000IU/ML) [RLD] -
Manufacturer: PFIZER
Approval date: March 15, 2022
Strength(s): 10,000IU/4ML (2,500IU/ML) [RLD]
Is there a generic version of Fragmin available?
No. There is currently no therapeutically equivalent version of Fragmin available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Fragmin. 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: Generic Drug FAQ.
More about Fragmin (dalteparin)
- Check interactions
- Compare alternatives
- Pricing & coupons
- Reviews (5)
- Side effects
- Dosage information
- During pregnancy
- Drug class: heparins
- Breastfeeding
- En español
Patient resources
Professional resources
Related treatment guides
Related/similar drugs
Heparin Sodium
Heparin Sodium is used for angina, anticoagulation during pregnancy, antiphospholipid syndrome ...
Lovenox
Lovenox is used to prevent deep vein thrombosis (DVT) which can lead to blood clots in the lungs ...
Botox
Botox is used for cosmetic purposes and to treat overactive bladder symptoms, urinary incontinence ...
Monoject Prefill Advanced
Monoject Prefill Advanced is used for patency maintenance of indwelling intravenous devices
Heparin
Heparin injection is used to treat and prevent blood clots in the veins, arteries, or lungs. Learn ...
Heparin flush
Heparin flush is used for patency maintenance of indwelling intravenous devices
Enoxaparin
Enoxaparin is used for acute coronary syndrome, angina, deep vein thrombosis, deep vein thrombosis ...
Dalteparin
Dalteparin is used for angina, deep vein thrombosis prophylaxis after abdominal surgery, deep vein ...
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. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.