A few years ago, after learning she had high blood pressure, Shannon Connell-Robichaud asked her doctor to switch her birth-control pill prescription. She had read that the pill she had been prescribed put people around her age with that condition at high risk of a stroke.The doctor agreed, she said — but only after Ms. Connell-Robichaud, a 32-year-old paralegal, shared a list of the blood-pressure measurements she had been keeping on her own. After that, she recalled, the doctor said, “Hey, maybe you’re right.”The question of whether women can monitor their own health risks in taking birth-control pills is at the heart of a debate now playing out in the pharmaceutical industry and at the Food and Drug Administration: Should oral contraceptives be made available over the counter rather than requiring a prescription?Though they are taken by millions of people, birth-control pills can interact with certain medical conditions in ways that have always placed them in the prescription category, meaning a doctor’s oversight is required.If the F.D.A. approves an over-the-counter version, it will be effectively saying that women with underlying health risks who choose that option will have to do their own research on how the birth-control pill would interact with their condition and any other medications they are taking.Reproductive-rights activists in the United States view an over-the-counter birth-control pill as an easy and effective tool for rural, poor and historically marginalized communities to avoid unwanted pregnancies — reducing their barriers to health care and lowering the abortion rate along the way.At least two drug companies want to apply to the F.D.A. to make the switch to an over-the-counter version, and have been in communication with the agency about their plans. But after years of preliminary trials to clear the agency’s research and consumer-testing hurdles, neither has reached the stage of applying yet.The F.D.A. defenders say that by asking many questions and demanding rigorous testing, the agency is being prudent about assessing the potential health risks of making the pill available without a prescription.But frustrated supporters of the switch are critical of the agency’s prolonged pre-application process — which at certain points requires F.D.A. permission to advance to the next stage. Some of them see the process as an obstacle to the advancement of reproductive rights, as well as a case study of the cost when the F.D.A. takes an overly cautious approach. (The agency has also been criticized in other drug-approval cases of moving too quickly, as when it fast-tracked approval of a controversial Alzheimer’s drug earlier this year.)Proponents of allowing over-the-counter access say they view the issue with greater urgency now that the Supreme Court is reconsidering the constitutional right to abortion as established by Roe v. Wade in 1973.The movement to enhance access to birth-control pills “is something that gives a bit of hope in these days where it feels we are constantly under attack,” Monica Simpson, executive director of the reproductive rights organization SisterSong, said in a webinar in late September.Oral contraceptives are already the most popular nonpermanent method of birth control in the United States and are sold over the counter in scores of countries, including the United Arab Emirates, China and Mexico.In the United States, close to $3 billion in prescription birth-control pills are sold each year, according to the life-sciences research firm Iqvia. They are manufactured by a variety of drug companies, including Pfizer Inc. and Bayer AG.The push to approve an over-the-counter option is coming primarily from two smaller players: Cadence Health, which is planning to apply on behalf of its oral contraceptive, Zena, and from HRA Pharma, a small drug maker based in Paris.Research shows that birth-control pills are safer than pregnancy itself, which carries a higher risk of blood clots, among other health concerns.“We want to make it safe. We are not trying to cut corners at all,” said Dr. Nap Hosang, the obstetrician and gynecologist who is co-chief executive of Cadence Health.But the process has been moving slowly, and the F.D.A., which has been in discussions since at least 2016 with both Cadence and HRA Pharma, has yet to be convinced.Dr. Nap Hosang, co-chief executive of Cadence Health, says the company isn’t going to cut corners for its over-the-counter pill.Carolyn Fong for The New York TimesHRA Pharma completed its final testing phase, known as the “actual-use trial,” this year. It is expected to file a formal application for over-the-counter approval next year. But the F.D.A. put the brakes on Cadence’s actual-use trial about a year ago. It has asked the company to consider adding new warnings and additional details to existing warnings on its drug-safety label, and to repeat some tests for over-the-counter use.Cadence officials say they are frustrated by the holdup. But one factor that may be working against Cadence is that Zena is a so-called combined pill, meaning it contains both estrogen and a progestin, whereas HRA Pharma’s pill contains only progesterone.Combined pills like Cadence’s account for 90 percent or more of oral contraceptive sales overall because they are less likely to cause unscheduled bleeding and require less vigilance on the part of patients to take them at the same time every day. But they also carry greater safety risks for some women, including those with high blood pressure or clotting issues, than their progestin-only counterparts, like HRA Pharma’s pill.“The sense that I have gotten, and it sounds like you have heard the same, is that F.D.A. has more questions about putting a combined pill over the counter,” said Dr. Susan Wood, a health-policy professor at George Washington University. She resigned as director of women’s health at the F.D.A. in 2005 over what she considered unreasonable delays in approving over-the-counter use of the drug Plan B, which prevents pregnancy after unprotected sex.“I don’t think they’re being political, I think they’re just being cautious,” she said. “They have to consider safety in an OTC setting,” which is different than safety in a prescription-only setting, she added.Still, Dr. Wood and other past participants in the F.D.A. switch process say that spending five years or more in a dialogue over testing and drug safety materials before a switch to over-the-counter availability has even been applied for — as Cadence and HRA Pharma have — is a strikingly long time.The F.D.A. declined to address specific questions about Cadence and HRA Pharma but said it aims to make a decision within 10 months once any company submits an application for approval of a move from prescription to over-the-counter status. “The amount of time that a company spends in its development program prior to submitting an application for a prescription-to-nonprescription switch is determined by the company, not by the F.D.A.,” an agency spokeswoman said in a statement.The two companies see it differently. They say they have sought the F.D.A.’s blessing — and have at points been obligated to have it in order to proceed — throughout their preparations. “We are required to get their clearance to move to the next step in development. And we don’t have their clearance,” said Samantha Miller, the co-chief executive of Cadence.Oral contraceptives are already the most popular nonpermanent method of birth control in the U.S. They are sold over the counter in many countries, including the United Arab Emirates, China and Mexico.Hannah Yoon for The New York TimesThe F.D.A.’s over-the-counter switch option appeals to some pharmaceutical companies because the first drug in its class to be switched can be granted three years of exclusivity in its market, giving it a temporary monopoly on over-the-counter sales. That advantage is one reason the larger Dublin, Ireland-based pharmaceutical company Perrigo announced plans earlier this year to acquire HRA Pharma. To varying degrees, both HRA Pharma and Cadence Health are involved with outside efforts to convince the F.D.A. to go along with their plans. While HRA Pharma has been publicly quiet about its interactions with the agency, it has worked closely with a research and advocacy group that is pushing the agency to approve an over-the-counter option. And Cadence is counting on women’s health providers and public-health officials to try to get the agency to look more favorably on its planned application.Last year, Cadence hired the Dallas-based consultant Rania Batrice, a deputy campaign manager to Senator Bernie Sanders during his 2016 presidential campaign, to advise it on a political strategy.Ms. Batrice has been urging lawmakers like Representative Barbara Lee, the California Democrat who co-chairs the Congressional Pro-Choice Caucus, to ask the F.D.A. to participate in a panel of medical experts to evaluate the idea of a switch to over-the-counter status for Zena.“Access to over-the-counter birth control is a racial equity issue, a gender equity issue, and an economic equity issue,” Ms. Lee said in a statement. “In the same way that other methods of birth control are available over the counter, the pill should be too.” “At this point there are now really some challenging issues that could prevent a successful OTC switch,” said Samantha Miller, Cadence Health’s co-chief executive officer.Carolyn Fong for The New York TimesMs. Batrice has also been working with grassroots organizations like the Indigenous rights group NDN Collective and the New American Leaders Action Fund to help carry the message that over-the-counter access to a drug like Zena would benefit rural residents, people of color and others with barriers to health care.But Cadence executives say approval for Zena is likely two years away at least — if they are successful at all with the F.D.A.“We’ve had so many issues discussed and agreed with this F.D.A. over the past five years,” said Ms. Miller. “At this point there are now really some challenging issues that could prevent a successful OTC switch.”Among them is opposition from anti-abortion groups like the Family Research Council and the American Association of Pro-Life Obstetricians and Gynecologists, which say that women’s reproductive health decisions should be made in consultation with a doctor. And some women say they are not sure the drugs should be freely available without a doctor or a pharmacist’s input.“I know so many people that don’t read the box, that don’t pay attention,” said Jordan de Jongh, who takes oral contraceptives. Callaghan O’Hare for The New York Times“I know so many people that don’t read the box, that don’t pay attention,” said Jordan de Jongh, a 28-year-old data-entry worker in Houston who takes oral contraceptives. “So I could see a teen girl getting access to birth control at a pharmacy without having to tell her super religious parents; that’s awesome. But I could see a girl taking five pills and thinking she won’t get pregnant from having sex last night; that’s a myth.”