Reviva Pharmaceuticals Holdings, Inc. (NASDAQ:RVPH – Get Free Report) has earned a consensus rating of “Moderate Buy” from the eight research firms that are currently covering the firm, Marketbeat.com reports. One analyst has rated the stock with a sell recommendation, two have assigned a hold recommendation and five have issued a buy recommendation on the company. The average 12 month price objective among analysts that have covered the stock in the last year is $66.6667.
Several research firms recently commented on RVPH. Weiss Ratings reaffirmed a “sell (e+)” rating on shares of Reviva Pharmaceuticals in a research report on Tuesday, April 21st. Wall Street Zen upgraded Reviva Pharmaceuticals from a “sell” rating to a “hold” rating in a report on Sunday, July 5th.
Read Our Latest Research Report on RVPH
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Reviva Pharmaceuticals Stock Performance
Shares of RVPH stock opened at $0.45 on Friday. Reviva Pharmaceuticals has a 52 week low of $0.26 and a 52 week high of $17.20. The company’s 50 day moving average price is $0.57 and its two-hundred day moving average price is $1.85. The company has a market capitalization of $5.90 million, a P/E ratio of -0.11 and a beta of 0.53.
Reviva Pharmaceuticals (NASDAQ:RVPH – Get Free Report) last released its quarterly earnings results on Thursday, May 14th. The company reported ($0.46) earnings per share for the quarter, missing the consensus estimate of ($0.36) by ($0.10). Analysts forecast that Reviva Pharmaceuticals will post -2.96 earnings per share for the current year.
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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