medique diamode

Generic: loperamide hydrochloride

Labeler: unifirst first aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name medique diamode
Generic Name loperamide hydrochloride
Labeler unifirst first aid corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loperamide hydrochloride 2 mg/1

Manufacturer
Unifirst First Aid Corporation

Identifiers & Regulatory

Product NDC 47682-200
Product ID 47682-200_441e7620-28e5-8cc5-e063-6394a90a2a72
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074091
Listing Expiration 2026-12-31
Marketing Start 2008-12-30

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47682200
Hyphenated Format 47682-200

Supplemental Identifiers

RxCUI
978010 978012
UPC
0347682200640
UNII
77TI35393C

Packaging Origin

Original Packager
true

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 medique diamode (source: ndc)
Generic Name loperamide hydrochloride (source: ndc)
Application Number ANDA074091 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 1 TABLET in 1 PACKET (47682-200-46)
  • 24 PACKET in 1 BOX, UNIT-DOSE (47682-200-64) / 1 TABLET in 1 PACKET (47682-200-46)
  • 6 PACKET in 1 BOX, UNIT-DOSE (47682-200-69) / 1 TABLET in 1 PACKET
source: ndc

Packages (3)

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": "441e7620-28e5-8cc5-e063-6394a90a2a72", "openfda": {"upc": ["0347682200640"], "unii": ["77TI35393C"], "rxcui": ["978010", "978012"], "spl_set_id": ["069e7979-a223-4819-b6cf-ea2731bf156b"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 PACKET (47682-200-46)", "package_ndc": "47682-200-46", "marketing_start_date": "20081230"}, {"sample": false, "description": "24 PACKET in 1 BOX, UNIT-DOSE (47682-200-64)  / 1 TABLET in 1 PACKET (47682-200-46)", "package_ndc": "47682-200-64", "marketing_start_date": "20081230"}, {"sample": false, "description": "6 PACKET in 1 BOX, UNIT-DOSE (47682-200-69)  / 1 TABLET in 1 PACKET", "package_ndc": "47682-200-69", "marketing_start_date": "20081230"}], "brand_name": "MEDIQUE Diamode", "product_id": "47682-200_441e7620-28e5-8cc5-e063-6394a90a2a72", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "47682-200", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MEDIQUE Diamode", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA074091", "marketing_category": "ANDA", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}