NDC 68001-0397-00
Famotidine 20 mg/1 TABLET, FILM COATED
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NDC
68001-0397-00
Generic Name
Famotidine
Brand Name
Famotidine
Strength
20 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
—
Labeler
BluePoint Laboratories
FDA Drug Information
Indications & Usage
1 INDICATIONS AND 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 duo…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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