loperamide hydrochloride
Generic: loperamide hydrochloride
Labeler: avpakDrug Facts
Product Profile
Brand Name
loperamide hydrochloride
Generic Name
loperamide hydrochloride
Labeler
avpak
Dosage Form
CAPSULE
Routes
Active Ingredients
loperamide hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-482
Product ID
50268-482_2b49645c-34d1-c6ab-e063-6394a90aaee5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215579
Listing Expiration
2026-12-31
Marketing Start
2023-04-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268482
Hyphenated Format
50268-482
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
ANDA215579 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-482-15) / 1 CAPSULE in 1 BLISTER PACK (50268-482-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b49645c-34d1-c6ab-e063-6394a90aaee5", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["f8992723-dd9a-bcf6-e053-6294a90aa65c"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-482-15) / 1 CAPSULE in 1 BLISTER PACK (50268-482-11)", "package_ndc": "50268-482-15", "marketing_start_date": "20230405"}], "brand_name": "Loperamide Hydrochloride", "product_id": "50268-482_2b49645c-34d1-c6ab-e063-6394a90aaee5", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "50268-482", "generic_name": "loperamide hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA215579", "marketing_category": "ANDA", "marketing_start_date": "20230405", "listing_expiration_date": "20261231"}