loperamide hydrochloride

Generic: loperamide hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loperamide hydrochloride
Generic Name loperamide hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loperamide hydrochloride 2 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8393
Product ID 68788-8393_69ab7391-0b01-4bc2-bedb-8959de130500
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206548
Listing Expiration 2026-12-31
Marketing Start 2023-03-01

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888393
Hyphenated Format 68788-8393

Supplemental Identifiers

RxCUI
978010
UNII
77TI35393C

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name loperamide hydrochloride (source: ndc)
Generic Name loperamide hydrochloride (source: ndc)
Application Number ANDA206548 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 CARTON (68788-8393-2) / 6 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

loperamide hydrochloride (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "69ab7391-0b01-4bc2-bedb-8959de130500", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["5b173bb9-3cca-44ce-9bcb-b9ecc93d3dcf"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (68788-8393-2)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "68788-8393-2", "marketing_start_date": "20230301"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68788-8393_69ab7391-0b01-4bc2-bedb-8959de130500", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68788-8393", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA206548", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}