Generic Septocaine Availability
Last updated on Aug 7, 2024.
Septocaine is a brand name of articaine/epinephrine, approved by the FDA in the following formulation(s):
SEPTOCAINE (articaine hydrochloride; epinephrine bitartrate - injectable;injection)
-
Manufacturer: DEPROCO
Approval date: April 3, 2000
Strength(s): 4%;EQ 0.017MG BASE/1.7ML (4%;EQ 0.01MG BASE/ML) [RLD] -
Manufacturer: DEPROCO
Approval date: March 30, 2006
Strength(s): 4%;EQ 0.0085MG BASE/1.7ML (4%;EQ 0.005MG BASE/ML) [RLD]
Has a generic version of Septocaine been approved?
An Authorized Generic version of Septocaine has been approved. An Authorized Generic is a prescription drug that is produced by a brand company under a New Drug Application (NDA) and marketed as a generic under a private label. It is identical to the branded product in appearance and has exactly the same inactive ingredients.
List of authorized generic versions:
- Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
Septodont, Inc.
NDC Code: 003620830 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
Henry Schein
NDC Code: 004046620 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .005 mg/mL; mg/mL
Henry Schein
NDC Code: 004046625 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
NDC, Inc.
NDC Code: 431280101 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .005 mg/mL; mg/mL
NDC, Inc.
NDC Code: 431280102 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
Patterson Dental
NDC Code: 502271040 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .005 mg/mL; mg/mL
Patterson Dental
NDC Code: 502271050 - Articaine hydrochloride and Epinephrine Bitartrate SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
Dentsply Pharmaceutical
NDC Code: 663120601 - Articaine hydrochloride and Epinephrine Bitartrate SUBMUCOSAL INJECTION, SOLUTION 40; .005 mg/mL; mg/mL
Dentsply Pharmaceutical
NDC Code: 663120602 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .01 mg/mL; mg/mL
Benco Dental
NDC Code: 669750417 - Articaine Hydrochloride and Epinephrine SUBMUCOSAL INJECTION, SOLUTION 40; .005 mg/mL; mg/mL
Benco Dental
NDC Code: 669750418
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Septocaine. 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 Septocaine (articaine / epinephrine)
- Check interactions
- Compare alternatives
- Reviews (5)
- Side effects
- Dosage information
- During pregnancy
- Drug class: local injectable anesthetics
- En español
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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
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