clorazepate dipotassium

Generic: clorazepate dipotassium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clorazepate dipotassium
Generic Name clorazepate dipotassium
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clorazepate dipotassium 15 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-256
Product ID 72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075731
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2000-04-27

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789256
Hyphenated Format 72789-256

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 ANDA075731 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)
source: ndc

Packages (1)

72789-256-06 6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)

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": "2e5c9777-8e42-bc90-e063-6294a90a1ee8", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["7b59a3ab-3dff-4458-a63a-ef0d9e0d996d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)", "package_ndc": "72789-256-06", "marketing_start_date": "20220701"}], "brand_name": "Clorazepate Dipotassium", "product_id": "72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-256", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA075731", "marketing_category": "ANDA", "marketing_start_date": "20000427", "listing_expiration_date": "20261231"}