Macrobid Generic Name: E: NITROFURANTOIN (nye-troe-fyoor-AN-toyn)

Macrodantin Generic Name: E: NITROFURANTOIN (nye-troe-fyoor-AN-toyn)

Marvelon 21

Maxalt Generic Name: E: RIZATRIPTAN (rye-za-TRIP-tan)

Maxalt-MLT Generic Name: E: RIZATRIPTAN (rye-za-TRIP-tan)

Maxidex Generic Name: DEXAMETHASONE (dex-a-METH-a-sone)

Mazindol (IFA-LOSE) Generic ingredient - Mazindol

Meclizine Generic Name: E: MECLIZINE (MEK-li-zeen)

Melatonin

Mellitron

Meridia (generic only Sibutramine) Chemical Name: SIBUTRAMINE (si-BYOO-tra-meen)

Mestinon Generic Name: E: PYRIDOSTIGMINE (peer-id-oh-STIG-meen)

Metformin Generic Name: E: METFORMIN (met-FOR-min)

Methotrexate Lederle Chemical Name: METHOTREXATE (meth-o-TREX-ate)

Metoprolol Generic Name: E: METOPROLOL (me-TOE-proe-lole)

Metrigen Fuerte

Metrocream 30gr Chemical Name: METRONIDAZOLE (me-troe-NI-da-zole)

Metrogel .75% topical gel Chemical Name: METRONIDAZOLE (me-troe-NI-da-zole)

Mevacor Generic Name: E: LOVASTATIN (LOE-va-sta-tin)

Mevacor (Generic) Chemical Name: LOVASTATIN (LOE-va-sta-tin)

Mevacor (generic) Generic Name: E: LOVASTATIN (LOE-va-sta-tin)

Micardis Chemical Name: TELMISARTAN (tel-mi-SAR-tan)

Micronase (generic) Generic Name: E: GLYBURIDE (GLYE-byoo-ride)

Microret

Minocin Chemical Name: MINOCYCLINE (mi-noe-SYE-kleen)

Minocycline Chemical Name: MINOCYCLINE (mi-noe-SYE-kleen)

Mircette (21 pills) 3 month (63 pills) supply Generic Name: E: DESOGESTREL (des-oh-JES-trel) and ETHINYL ESTRADIOL (ETH-in-il ess-tra-DYE-ole)

Mizonal

Mobic 7.5 mg Generic Name: E: MELOXICAM (mee-LOX-i-kam)

Moduretic Generic Name: E: AMILORIDE (a-MILL-oh-ride) and HYDROCHLOROTHIAZIDE (hye-droe-klor-oh-THYE-a-zide)

Monopril Generic Name: E: FOSINOPRIL (foe-SIN-oh-pril)

Motilium

Motrin Generic Name: E: IBUPROFEN (eye-byoo-PROE-fen)

MVI-12

Mycostatin Generic Name: E: NYSTATIN (nye-STAT-in)

Mycostatin 60gr Generic Name: E: NYSTATIN (nye-STAT-in)

Mysoline Generic Name: E: PRIMIDONE (PRYE-mih-done)

METOLAR (Betaloc, Lopressor, Metoprolol Tartrate, Toprol)

MOBIC ( Meloxicam )

MODAPRO ( Modalert, Modafinil, Provigil )

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FDA Warns on Black-Market IUDs : WASHINGTON -- Many intrauterine devices (IUDs) sold over the Internet from foreign pharmacies are not approved in the U.S. and are possibly dangerous, the FDA said. The agency said an investigation disclosed that patients in Rhode Island, Massachusetts, and Kentucky had received unapproved IUDs from healthcare providers who had bought them from foreign pharmacies, presumably to save money. In a "Dear Colleague" letter to providers, the FDA said it had uncovered distribution of "unapproved versions of FDA-approved products such as Mirena, Implanon, Copper-T, and ParaGard; as well as products not approved for use in the U.S., such as T-Safe." These products may not be as effective or safe as FDA-approved IUDs, the agency warned. Women who believe they may have received an unapproved IUD should use another contraceptive method and talk to their healthcare providers, the FDA recommended. The FDA also advised physicians to use extra caution when asked to insert IUDs provided by patients. Healthcare providers should verify that products are authentic FDA-approved devices and were purchased from a licensed U.S.-based supplier. The agency also noted that billing Medicaid or private insurers for unapproved medical products could bring criminal fraud charges. "To reduce the chance of receiving an unapproved or adulterated medical product, your Internet purchases should be made from state-licensed distributors or pharmacies located in the U.S.," the FDA said. It recommended buying only from Internet pharmacies displaying a logo from the National Association of Boards of Pharmacy, known as the VIPPS seal for Verified Internet Pharmacy Practice Sites. "Healthcare providers should be aware that purchasing medical products from websites that are outside of the U.S. may be illegal and may increase the risk of receiving a potentially harmful product, since many websites sell products that are not FDA approved and could be manufactured in other countries." The FDA first became aware of the problem in Rhode Island, but its probe turned up unapproved products in the two other states. The investigation is continuing, the agency said.

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