LEVAQUIN- levofloxacin tablet, film coated United States - English - NLM (National Library of Medicine)

levaquin- levofloxacin tablet, film coated

redpharm drug inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin - unii:6gnt3y5lmf) - levofloxacin 250 mg - to reduce the development of drug-resistant bacteria and maintain the effectiveness of levaquin® and other antibacterial drugs, levaquin® should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. levaquin® tablets/injection and oral solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. levaquin® injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). culture and susceptibility testing appropriate culture and

LEVAQUIN- levofloxacin tablet, film coated United States - English - NLM (National Library of Medicine)

levaquin- levofloxacin tablet, film coated

redpharm drug inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin - unii:6gnt3y5lmf) - levofloxacin 500 mg - to reduce the development of drug-resistant bacteria and maintain the effectiveness of levaquin® and other antibacterial drugs, levaquin® should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. levaquin® tablets/injection and oral solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. levaquin® injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). culture and susceptibility testing appropriate culture and

LEVAQUIN- levofloxacin tablet, film coated United States - English - NLM (National Library of Medicine)

levaquin- levofloxacin tablet, film coated

redpharm drug inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin - unii:6gnt3y5lmf) - levofloxacin 750 mg - to reduce the development of drug-resistant bacteria and maintain the effectiveness of levaquin® and other antibacterial drugs, levaquin® should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. levaquin® tablets/injection and oral solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. levaquin® injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). culture and susceptibility testing appropriate culture and

LEVAQUIN- levofloxacin tablet, film coated United States - English - NLM (National Library of Medicine)

levaquin- levofloxacin tablet, film coated

rebel distributors corp - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin - unii:6gnt3y5lmf) - levofloxacin 500 mg - to reduce the development of drug-resistant bacteria and maintain the effectiveness of levaquin® and other antibacterial drugs, levaquin® should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. when culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. levaquin® tablets/injection and oral solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. levaquin® injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). culture and susceptibility testing appropriate culture and

NUCYNTA- tapentadol hydrochloride tablet, film coated United States - English - NLM (National Library of Medicine)

nucynta- tapentadol hydrochloride tablet, film coated

physicians total care, inc. - tapentadol hydrochloride (unii: 71204kii53) (tapentadol - unii:h8a007m585) - tapentadol hydrochloride 50 mg - nucynta® (tapentadol) is indicated for the relief of moderate to severe acute pain in patients 18 years of age or older. enter section text here like other drugs with mu-opioid agonist activity, nucynta® is contraindicated in patients with significant respiratory depression in unmonitored settings or the absence of resuscitative equipment. nucynta® is also contraindicated in patients with acute or severe bronchial asthma or hypercapnia in unmonitored settings or the absence of resuscitative equipment [see warnings and precautions (5.1)] . like drugs with mu-opioid agonist activity, nucynta® is contraindicated in any patient who has or is suspected of having paralytic ileus. nucynta® is contraindicated in patients who are receiving monoamine oxidase (mao) inhibitors or who have taken them within the last 14 days due to potential additive effects on norepinephrine levels which may result in adverse cardiovascular events [see drug interactions (7.4)] . enter section text here pregnancy category c

mycelex- clotrimazole troche United States - English - NLM (National Library of Medicine)

mycelex- clotrimazole troche

bayer pharmaceuticals corp - clotrimazole (unii: g07gz97h65) - troche - 10 mg - mycelex® troches are indicated for the local treatment of oropharyngeal candidiasis.the diagnosis should be confirmed by a koh smear and/or culture prior to treatment. mycelex® troches are also indicated prophylactically to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia, solid tumors, or renal transplantation. there are no data from adequate and well-controlled trials to establish the safety and efficacy of this product for prophylactic use in patients immunocompromised by etiologies other than those listed in the previous sentence. (see dosage and administration .) mycelex® troches are contraindicated in patients who are hypersensitive to any of its components. no data available.

SALINE- nasal spray United States - English - NLM (National Library of Medicine)

saline- nasal spray

raritan pharmaceuiticals inc - sodium chloride 0.65% - moisturizer naturally provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

DRX CHOICE STOMACH RELIEF REGULAR STRENGTH- bismuth subsalicylate suspension United States - English - NLM (National Library of Medicine)

drx choice stomach relief regular strength- bismuth subsalicylate suspension

raritan phamaceuticals inc - bismuth subsalicylate (unii: 62tey51rr1) (bismuth cation - unii:zs9cd1i8ye, salicylic acid - unii:o414pz4lpz) - upset stomach reliever and antidiarrheal relieves

OVERNIGHT COLD AND FLU- acetaminophen, dextromethorphan hbr, triprolidine hcl solution United States - English - NLM (National Library of Medicine)

overnight cold and flu- acetaminophen, dextromethorphan hbr, triprolidine hcl solution

raritan pharmaceuticals - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), dextromethorphan hydrobromide (unii: 9d2rti9kyh) (dextromethorphan - unii:7355x3rots), triprolidine hydrochloride (unii: yan7r5l890) (triprolidine - unii:2l8t9s52qm) -

DRX CHOICE CHILDREN DAYTIME COUGH AND CHEST CONGESTION- dextromethorphan hbr and guaifenesin liquid United States - English - NLM (National Library of Medicine)

drx choice children daytime cough and chest congestion- dextromethorphan hbr and guaifenesin liquid

raritan pharmaceuticals - dextromethorphan hydrobromide (unii: 9d2rti9kyh) (dextromethorphan - unii:7355x3rots), guaifenesin (unii: 495w7451vq) (guaifenesin - unii:495w7451vq) - cough suppressant expectorant if you are now taking a prescription monoamine oxidase inhibitor (maoi) (certain drugs for depression, psychiatric, or emotional conditions, or parkinson's disease), or for 2 weeks after stopping the maoi drug. if you do not know if your child's prescription drug contains an maoi, ask a doctor or pharmacist before taking this product. cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. these could be signs of a serious condition.