Lasix is a brand name of furosemide, approved by the lasix generic name FDA in the following formulation(s lasix (furosemide lasix high - injectable;injection manufacturer: sanofi aventis US, approved Prior to tikosyn and lasix Jan 1, 1982. Strength(s 10MG/ML, rLD, lasix (furosemide - solution;oral manufacturer: sanofi aventis US, approved Prior to Jan 1, 1982. Strength(s 10MG/ML, lasix (furosemide - tablet;oral manufacturer: US pharm holdings. Approved Prior to Jan 1, 1982. Strength(s 20MG, rLD, aB, 40MG, rLD, aB, 80MG. RLD, aB, has a generic version of Lasix been approved? The following products are equivalent to Lasix: furosemide tablet;oral, manufacturer: ipca labs LTD, approval date: September 18, 2006. Strength(s 20MG, aB, 40MG, aB, 80MG,. Manufacturer: ivax SUB lasix generic name teva pharms, approval date: November 30, 1983, strength(s 20MG, aB, 40MG,. Manufacturer: leading pharma LLC Approval date: November 9, 2005 Strength(s 20MG AB, 40MG AB, 80MG AB Manufacturer: mylan Approved Prior to Jan 1, 1982 Strength(s 20MG AB, 40MG AB Manufacturer: mylan Approval date: October 29, 1986 Strength(s 80MG AB Manufacturer: prinston INC Approval date: March. Furosemide - injectable;injection furosemide - solution;oral Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Lasix. 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. Add to My Med List More about Lasix (furosemide) Consumer resources Professional resources Related treatment guides Glossary Term Definition Drug Patent A drug renal flow scan with lasix lasix 40 mg tablets patent is assigned by the.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, what type of diuretic is lasix ingredient lasix generic name formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can. 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. RLeference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (anda). By designating a single reference lasix generic name listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. 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 lasix injection administration 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. Generic Name: furosemide (fur OH se mide brand Names: Lasix, Diaqua-2, Lo-Aqua, medically reviewed on December 27, 2017.
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Edema, therapy should be individualized according lasix mg to patient response to gain maximal therapeutic response and to determine the minimal dose lasix mg needed to maintain that response. Adults - The usual initial lasix mg dose of lasix is 20 lasix mg to 80mg given as a single dose. Ordinarily a prompt diuresis ensues. If needed, the same dose can be administered 6 to 8 hours later or the dose may lasix mg be increased. The dose may be raised by 20 or 40mg and given not sooner than 6 to 8 hours after the previous dose until the desired diuretic effect has been obtained. The individually determined single dose should then be given once or twice daily (e.g., at 8 am and 2 pm). The dose of lasix may be carefully titrated up to 600 mg/day in patients with clinically severe edematous states. Edema may be most efficiently and safely mobilized by giving lasix on 2 to 4 consecutive days each week. When doses exceeding 80 mg/day are given for prolonged periods, careful clinical observation and laboratory monitoring are particularly advisable (see. Precautions: Laboratory Test ). Geriatric patients - In general, dose selection for the elderly patient should be cautious, usually starting at the low end of the dosing range (see. Precautions: Geriatric Use ). Pediatric patients - The usual initial dose of oral lasix in pediatric patients is 2 mg/kg body weight, given as a single dose. If the diuretic response is not satisfactory after the initial dose, dosage may be increased by 1 or 2 mg/kg no sooner than 6 to 8 hours after the previous dose. Doses greater than 6 mg/kg body weight are not recommended. For maintenance therapy in pediatric patients, the dose should be adjusted to the minimum effective level. Hypertension, therapy should be individualized according to the patients response to gain maximal therapeutic response and to determine the minimal dose needed to maintain the therapeutic response. Adults - The usual initial dose of lasix for hypertension is 80mg, usually divided into 40mg twice a day. Dosage should then be adjusted according to response. If response is not satisfactory, add other antihypertensive agents. Changes in blood pressure must be carefully monitored when lasix is used with other antihypertensive drugs, especially during initial therapy. To prevent excessive drop in blood pressure, the dosage of other agents should be reduced by at least 50 when lasix is added to the regimen. As the blood pressure falls under the potentiating effect of lasix, a further reduction in dosage or even discontinuation of other antihypertensive drugs may be necessary. Geriatric patients - In general, dose selection and dose adjustment for the elderly patient should be cautious, usually starting at the low end of the dosing range (see. Dosage Form: tablet, medically reviewed on July 1, 2017, show On This Page, view All. Warning, furosemide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required and dose and dose schedule must be adjusted to the individual patients needs (See. Dosage AND administration ). Description, each tablet for oral administration contains: Furosemide USP. 20 mg, 40 mg and. Each mL of Oral Solution for oral administration contains: Furosemide USP. 10 mg per mL or 8 mg (40 mg per 5 mL). Furosemide is a diuretic which is an anthranilic acid derivative. Chemically, it is acid. Furosemide is a white to slightly yellow, crystalline powder. It is practically insoluble in water, sparingly soluble in alcohol, freely soluble in dilute alkali solutions and insoluble in dilute acids. The CAS Registry Number is 54-31-9. The structural formula is as follows: C12H11ClN2O5S.W. 330.74, furosemide Tablets USP are available for oral administration containing 20 mg, 40 mg or 80 mg of Furosemide USP. The tablets meet Dissolution Test. Each tablet contains the following inactive ingredients: colloidal silicon dioxide, corn starch, lactose monohydrate, microcrystalline cellulose, pregelatinized starch, purified water, sodium lauryl sulfate, sodium starch glycolate and stearic acid. Furosemide Oral Solution USP is also available for oral administration containing either 10 mg per mL or 40 mg per. The oral solution contains the following inactive ingredients: D and C Yellow. 10, FD and C Yellow. 6, flavors, potassium carbonate 1 hydrate, propylene glycol, purified water and sorbitol solution.
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