famotidine 20 mg
1 INDICATIONS & USAGE Famotidine tablets are indicated in adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer (GU). symptomatic nonerosive gastroesophageal reflux disease (GERD). erosive esophagitis due to GERD, diagnosed by biopsy. Famotidine tablets are indicated in adults for the: treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). reduction of the risk of duodenal ulcer recurrence. Famotidine is a histamine-2 (H2) receptor antagonist indicated (1) : In adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer. symptomatic nonerosive gastroesophageal reflux disease (GERD). erosive esophagitis due to GERD, diagnosed by biopsy. In adults for the: treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). reduction of the risk of DU recurrence.
ascend laboratories, llc
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16 HOW SUPPLIED/STORAGE AND HANDLING
FAMOTIDINE tablets are supplied as follows: NDC Strength Quantity Description 67877-842-01 20 mg 100 tablets in 1 HDPE container round, white to off-white film-coated tablets, debossed with āVā on one side and ā15ā on the other side. 67877-842-10 1000 tablets in 1 HDPE container round, white to off-white film-coated tablets, debossed with āVā on one side and ā15ā on the other side. 67877-889-01 40 mg 100 tablets in 1 HDPE container round, white to off-white film-coated tablets, debossed with āVā on one side and ā45ā on the other side. 67877-889-05 500 tablets in 1 HDPE container round, white to off-white film-coated tablets, debossed with āVā on one side and ā45ā on the other side. Storage Store at 25Ā°C (77Ā°F); excursions permitted to 15-30Ā°C (59-86Ā°F) (See USP Controlled Room Temperature). Dispense in a USP tight, light-resistant container.
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