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NDC 50090-3888-00 Famotidine 40 mg/1 Details
Famotidine 40 mg/1
Famotidine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is FAMOTIDINE.
MedlinePlus Drug Summary
Prescription famotidine is used to treat ulcers (sores on the lining of the stomach or small intestine); gastroesophageal reflux disease (GERD, a condition in which backward flow of acid from the stomach causes heartburn and injury of the esophagus [tube that connects the mouth and stomach]); and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome (tumors in the pancreas or small intestine that cause increased production of stomach acid). Over-the-counter famotidine is used to prevent and treat heartburn due to acid indigestion and sour stomach caused by eating or drinking certain foods or drinks. Famotidine is in a class of medications called H2 blockers. It works by decreasing the amount of acid made in the stomach.
Related Packages: 50090-3888-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Famotidine
Product Information
NDC | 50090-3888 |
---|---|
Product ID | 50090-3888_5f992a67-0f93-4457-8bcf-2b045c20a31d |
Associated GPIs | 49200030000340 |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Famotidine |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Famotidine |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 40 |
Active Ingredient Units | mg/1 |
Substance Name | FAMOTIDINE |
Labeler Name | A-S Medication Solutions |
Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA206530 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50090-3888-00 (50090388800)
NDC Package Code | 50090-3888-0 |
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Billing NDC | 50090388800 |
Package | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3888-0) |
Marketing Start Date | 2018-11-30 |
NDC Exclude Flag | N |
Pricing Information | N/A |