Shares of Reviva Pharmaceuticals Holdings, Inc. (NASDAQ:RVPH – Get Free Report) have been given a consensus recommendation of “Moderate Buy” by the eight analysts that are currently covering the stock, MarketBeat.com reports. One investment analyst has rated the stock with a sell rating, two have assigned a hold rating and five have given a buy rating to the company. The average 1 year target price among brokerages that have issued ratings on the stock in the last year is $66.6667.
Several equities analysts recently commented on RVPH shares. Maxim Group reissued a “hold” rating on shares of Reviva Pharmaceuticals in a report on Wednesday. Chardan Capital reissued a “buy” rating and issued a $40.00 target price on shares of Reviva Pharmaceuticals in a report on Monday, January 5th. Weiss Ratings reissued a “sell (e+)” rating on shares of Reviva Pharmaceuticals in a report on Thursday, January 22nd. D. Boral Capital lowered Reviva Pharmaceuticals from a “buy” rating to a “hold” rating in a report on Thursday, March 5th. Finally, HC Wainwright restated a “buy” rating and issued a $80.00 price objective on shares of Reviva Pharmaceuticals in a research note on Tuesday, December 23rd.
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Reviva Pharmaceuticals Price Performance
NASDAQ:RVPH opened at $0.79 on Monday. The firm has a market capitalization of $10.12 million, a PE ratio of -0.09 and a beta of 0.64. The business’s fifty day moving average price is $3.35 and its 200 day moving average price is $7.48. Reviva Pharmaceuticals has a 12 month low of $0.59 and a 12 month high of $23.20.
Reviva Pharmaceuticals Company Profile
Reviva Pharmaceuticals, Inc (NASDAQ: RVPH) is a specialty pharmaceutical company focused on the acquisition, development and commercialization of prescription drug products in the United States and select international markets. Founded in 2002 and headquartered in Coral Gables, Florida, Reviva targets under-promoted, off-patent pharmaceuticals for which novel dosage forms can enhance patient compliance and therapeutic outcomes.
The company’s core activities include the identification of FDA-approved drug candidates, formulation development to address niche or underserved patient populations—such as pediatric and orphan indications—and supporting regulatory filings.
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