Generic Rimactane Availability
Rimactane is a brand name of rifampin, approved by the FDA in the following formulation(s):
RIMACTANE (rifampin - capsule;oral)
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Manufacturer: OXFORD PHARMS
Approved Prior to Jan 1, 1982
Strength(s): 300MG [AB]
Has a generic version of Rimactane been approved?
Yes. The following products are equivalent to Rimactane:
rifampin capsule;oral
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Manufacturer: AKORN
Approval date: March 14, 2001
Strength(s): 300MG [AB] -
Manufacturer: LANNETT CO INC
Approval date: March 28, 2008
Strength(s): 300MG [AB] -
Manufacturer: LUPIN PHARMS
Approval date: August 21, 2013
Strength(s): 300MG [AB] -
Manufacturer: SANDOZ
Approval date: May 28, 1997
Strength(s): 300MG [AB]
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Rimactane. 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 FAQs.
More about Rimactane (rifampin)
- Rimactane Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Drug Interactions
- Support Group
- 0 Reviews – Add your own review/rating
- Generic Availability
- Drug class: rifamycin derivatives
Consumer resources
Other brands: Rifadin, Rifadin IV
Professional resources
Related treatment guides
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. |
| AB | Products meeting necessary bioequivalence requirements. Multisource drug products listed under the same heading (i.e., identical active ingredients(s), dosage form, and route(s) of administration) and having the same strength (see Therapeutic Equivalence-Related Terms, Pharmaceutical Equivalents) generally will be coded AB if a study is submitted demonstrating bioequivalence. In certain instances, a number is added to the end of the AB code to make a three character code (i.e., AB1, AB2, AB3, etc.). Three-character codes are assigned only in situations when more than one reference listed drug of the same strength has been designated under the same heading. Two or more reference listed drugs are generally selected only when there are at least two potential reference drug products which are not bioequivalent to each other. If a study is submitted that demonstrates bioequivalence to a specific listed drug product, the generic product will be given the same three-character code as the reference listed drug it was compared against. |
