loperamide hydrochloride
Generic: loperamide hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
loperamide hydrochloride
Generic Name
loperamide hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
loperamide hydrochloride 2 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888393
Hyphenated Format
68788-8393
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (68788-8393-2) / 6 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (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"}