loperamide hydrochloride
Generic: loperamide hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
loperamide hydrochloride
Generic Name
loperamide hydrochloride
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
loperamide hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-229
Product ID
60687-229_437e8cc1-d818-dac5-e063-6294a90a1752
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073192
Listing Expiration
2026-12-31
Marketing Start
2017-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687229
Hyphenated Format
60687-229
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
ANDA073192 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-229-01) / 1 CAPSULE in 1 BLISTER PACK (60687-229-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437e8cc1-d818-dac5-e063-6294a90a1752", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["42989f90-8ff5-44d1-a462-28c18ce02738"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-229-01) / 1 CAPSULE in 1 BLISTER PACK (60687-229-11)", "package_ndc": "60687-229-01", "marketing_start_date": "20170103"}], "brand_name": "Loperamide Hydrochloride", "product_id": "60687-229_437e8cc1-d818-dac5-e063-6294a90a1752", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "60687-229", "generic_name": "Loperamide Hydrochloride", "labeler_name": "American Health Packaging", "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": "20170103", "listing_expiration_date": "20261231"}