loperamide hydrochloride

Generic: loperamide hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loperamide hydrochloride
Generic Name loperamide hydrochloride
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

loperamide hydrochloride 2 mg/1

Manufacturer
American Health Packaging

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
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687229
Hyphenated Format 60687-229

Supplemental Identifiers

RxCUI
978006
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 ANDA073192 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-229-01) / 1 CAPSULE in 1 BLISTER PACK (60687-229-11)
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": "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"}