clorazepate dipotassium

Generic: clorazepate dipotassium

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clorazepate dipotassium
Generic Name clorazepate dipotassium
Labeler coupler llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clorazepate dipotassium 15 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1462
Product ID 67046-1462_2d5938fe-3981-3cd5-e063-6394a90a99a9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213730
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-02-04

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461462
Hyphenated Format 67046-1462

Supplemental Identifiers

RxCUI
197464
UNII
63FN7G03XY

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 clorazepate dipotassium (source: ndc)
Generic Name clorazepate dipotassium (source: ndc)
Application Number ANDA213730 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1462-3)
source: ndc

Packages (1)

67046-1462-3 30 TABLET in 1 BLISTER PACK (67046-1462-3)

Ingredients (1)

clorazepate dipotassium (15 mg/1)

Linked Drug Pages (1)

Clorazepate Dipotassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d5938fe-3981-3cd5-e063-6394a90a99a9", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["2d592a27-f4cf-008a-e063-6394a90a2629"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1462-3)", "package_ndc": "67046-1462-3", "marketing_start_date": "20250204"}], "brand_name": "Clorazepate Dipotassium", "product_id": "67046-1462_2d5938fe-3981-3cd5-e063-6394a90a99a9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "67046-1462", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA213730", "marketing_category": "ANDA", "marketing_start_date": "20250204", "listing_expiration_date": "20261231"}