SUCRALFATE tablet Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

sucralfate tablet

advanced rx pharmacy of tennessee, llc - sucralfate (unii: xx73205dh5) (sucralfate - unii:xx73205dh5) - sucralfate is indicated in: - short-term treatment (up to 8 weeks) of active duodenal ulcer. while healing with sucralfate may occur during the first week or two, treatment should be continued for 4 to 8 weeks unless healing has been demonstrated by x-ray or endoscopic examination. - maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. sucralfate is contraindicated in patients with known hypersensitivity reactions to the active substance or to any of the excipients.

SUCRALFATE-1 - TAB 1G TABLET Kanāda - angļu - Health Canada

sucralfate-1 - tab 1g tablet

pro doc limitee - sucralfate - tablet - 1g - sucralfate 1g - protectants

SUCRALFATE suspension Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

sucralfate suspension

atlantic biologicals corp. - sucralfate (unii: xx73205dh5) (sucralfate - unii:xx73205dh5) - sucralfate oral suspension is indicated in the short-term (up to 8 weeks) treatment of active duodenal ulcer. sucralfate oral suspension is contraindicated for patients with known hypersensitivity reactions to the active substance or to any of the excipients.

SUCRALFATE suspension Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

sucralfate suspension

pacific pharma, inc. - sucralfate (unii: xx73205dh5) (sucralfate - unii:xx73205dh5) - sucralfate oral suspension is indicated in the short-term (up to 8 weeks) treatment of active duodenal ulcer. sucralfate oral suspension is contraindicated for patients with known hypersensitivity reactions to the active substance or to any of the excipients.

Alsucral Jaunzēlande - angļu - Medsafe (Medicines Safety Authority)

alsucral

pacific pharmaceuticals limited (part of mylan) - sucralfate 0.5 g - chewable tablet - 0.5 g - active: sucralfate 0.5 g

Alsucral  (Pacific) Jaunzēlande - angļu - Medsafe (Medicines Safety Authority)

alsucral (pacific)

pacific pharmaceuticals limited (part of mylan) - sucralfate - tablet - 0.5g, 1.0g - active: sucralfate

Alsucral Powder Jaunzēlande - angļu - Medsafe (Medicines Safety Authority)

alsucral powder

pacific pharmaceuticals limited (part of mylan) - sucralfate 1 g - powder for oral solution - 1 g - active: sucralfate 1 g

TEVA-SUCRALFATE TABLET Kanāda - angļu - Health Canada

teva-sucralfate tablet

teva canada limited - sucralfate - tablet - 1g - sucralfate 1g - protectants

APO-SUCRALFATE - TAB 1G TABLET Kanāda - angļu - Health Canada

apo-sucralfate - tab 1g tablet

apotex inc - sucralfate - tablet - 1g - sucralfate 1g - protectants

CARAFATE- sucralfate suspension Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

carafate- sucralfate suspension

allergan, inc. - sucralfate (unii: xx73205dh5) (sucralfate - unii:xx73205dh5) - sucralfate 1 g in 10 ml - carafate (sucralfate) oral suspension is indicated in the short-term (up to 8 weeks) treatment of active duodenal ulcer. carafate oral suspension is contraindicated for patients with known hypersensitivity reactions to the active substance or to any of the excipients.