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NDC 50580-0134-04 Imodium 1 mg/7.5mL Details
Imodium 1 mg/7.5mL
Imodium is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is LOPERAMIDE HYDROCHLORIDE.
MedlinePlus Drug Summary
Nonprescription (over-the-counter) loperamide is used to control acute diarrhea (loose stools that come on suddenly and usually lasts less than 2 weeks), including travelers' diarrhea. Prescription loperamide is also used to control acute diarrhea and also ongoing diarrhea associated with inflammatory bowel disease (IBD; condition in which the lining of all or part of the intestine is swollen, irritated, or has sores). Prescription loperamide is also used to reduce the amount of fluid in people with ileostomies (surgery to create an opening for waste to leave the body through the abdomen). Loperamide is in a class of medications called antidiarrheal agents. It works by decreasing the flow of fluids and electrolytes into the bowel and by slowing down the movement of the bowel to decrease the number of bowel movements.
Related Packages: 50580-0134-04Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Loperamide
Product Information
| NDC | 50580-0134 |
|---|---|
| Product ID | 50580-134_f7555a4a-ab6c-65bc-e053-6394a90a483f |
| Associated GPIs | 47100020100902 |
| GCN Sequence Number | 059430 |
| GCN Sequence Number Description | loperamide HCl LIQUID 1MG/7.5ML ORAL |
| HIC3 | D6D |
| HIC3 Description | ANTIDIARRHEALS |
| GCN | 25065 |
| HICL Sequence Number | 001236 |
| HICL Sequence Number Description | LOPERAMIDE HCL |
| Brand/Generic | Brand |
| Proprietary Name | Imodium |
| Proprietary Name Suffix | A-D |
| Non-Proprietary Name | Loperamide Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/7.5mL |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Labeler Name | Johnson & Johnson Consumer Inc. |
| Pharmaceutical Class | Opioid Agonist [EPC], Opioid Agonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA019487 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50580-0134-04 (50580013404)
| NDC Package Code | 50580-134-04 |
|---|---|
| Billing NDC | 50580013404 |
| Package | 120 mL in 1 BOTTLE (50580-134-04) |
| Marketing Start Date | 2004-07-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |