loperamide hydrochloride
Generic: loperamide hydrochloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
loperamide hydrochloride
Generic Name
loperamide hydrochloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
loperamide hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2257
Product ID
68071-2257_1d76879d-380f-2f39-e063-6294a90ac055
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073192
Listing Expiration
2026-12-31
Marketing Start
1993-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712257
Hyphenated Format
68071-2257
Supplemental Identifiers
RxCUI
UPC
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
ANDA073192 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 6 CAPSULE in 1 BOTTLE (68071-2257-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d76879d-380f-2f39-e063-6294a90ac055", "openfda": {"upc": ["0368071225761"], "unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["af0b886f-c065-26dc-e053-2995a90ac471"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE in 1 BOTTLE (68071-2257-6)", "package_ndc": "68071-2257-6", "marketing_start_date": "20200911"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68071-2257_1d76879d-380f-2f39-e063-6294a90ac055", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-2257", "generic_name": "Loperamide Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA073192", "marketing_category": "ANDA", "marketing_start_date": "19930501", "listing_expiration_date": "20261231"}