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NDC 49035-0118-90 Famotidine 10 mg/1 Details
Famotidine 10 mg/1
Famotidine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores Inc. 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: 49035-0118-90Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Famotidine
Product Information
| NDC | 49035-0118 |
|---|---|
| Product ID | 49035-118_cc861603-d1e2-9af2-3b81-f1e9cae7c71d |
| Associated GPIs | 49200030000310 |
| GCN Sequence Number | 021688 |
| GCN Sequence Number Description | famotidine TABLET 10 MG ORAL |
| HIC3 | Z2D |
| HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
| GCN | 46432 |
| HICL Sequence Number | 004521 |
| HICL Sequence Number Description | FAMOTIDINE |
| Brand/Generic | Generic |
| Proprietary Name | Famotidine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Famotidine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | FAMOTIDINE |
| Labeler Name | Wal-Mart Stores Inc |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077367 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 49035-0118-90 (49035011890)
| NDC Package Code | 49035-118-90 |
|---|---|
| Billing NDC | 49035011890 |
| Package | 1 BOTTLE in 1 CARTON (49035-118-90) / 90 TABLET in 1 BOTTLE |
| Marketing Start Date | 2012-07-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |