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NDC 65162-0249-50 Alosetron Hydrochloride 1 mg/1 Details
Alosetron Hydrochloride 1 mg/1
Alosetron Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is ALOSETRON HYDROCHLORIDE.
MedlinePlus Drug Summary
Alosetron is used to treat diarrhea, pain, cramps, and the feeling of an urgent need to have bowel movements caused by irritable bowel syndrome (IBS; a condition that causes stomach pain, bloating, constipation, and diarrhea) in women who have diarrhea as their main symptom and have not been helped by other treatments. Alosetron is in a class of medications called 5-HT3 receptor antagonists. Alosetron works by slowing the movement of stool (bowel movements) through the intestines.
Related Packages: 65162-0249-50Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Alosetron
Product Information
| NDC | 65162-0249 |
|---|---|
| Product ID | 65162-249_bda445ca-01a9-40ee-aaf7-f8d6a321c01d |
| Associated GPIs | 52554015100320 |
| GCN Sequence Number | 044634 |
| GCN Sequence Number Description | alosetron HCl TABLET 1 MG ORAL |
| HIC3 | D6C |
| HIC3 Description | IRRITABLE BOWEL SYNDROME AGENTS, 5-HT3 ANTAGONIST |
| GCN | 41607 |
| HICL Sequence Number | 020953 |
| HICL Sequence Number Description | ALOSETRON HCL |
| Brand/Generic | Generic |
| Proprietary Name | Alosetron Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Alosetron Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/1 |
| Substance Name | ALOSETRON HYDROCHLORIDE |
| Labeler Name | Amneal Pharmaceuticals LLC |
| Pharmaceutical Class | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA206647 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65162-0249-50 (65162024950)
| NDC Package Code | 65162-249-50 |
|---|---|
| Billing NDC | 65162024950 |
| Package | 500 TABLET, FILM COATED in 1 BOTTLE (65162-249-50) |
| Marketing Start Date | 2017-01-02 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |