clorazepate dipotassium

Generic: clorazepate dipotassium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clorazepate dipotassium
Generic Name clorazepate dipotassium
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clorazepate dipotassium 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2100
Product ID 72162-2100_3f1acd4a-bbff-4e37-9f42-d05597821589
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215566
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-09-22

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622100
Hyphenated Format 72162-2100

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 ANDA215566 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2100-1)
source: ndc

Packages (1)

Ingredients (1)

clorazepate dipotassium (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f1acd4a-bbff-4e37-9f42-d05597821589", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["7fccd0b7-1abc-4c52-88e3-af7b7cc079a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2100-1)", "package_ndc": "72162-2100-1", "marketing_start_date": "20220922"}], "brand_name": "Clorazepate Dipotassium", "product_id": "72162-2100_3f1acd4a-bbff-4e37-9f42-d05597821589", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72162-2100", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA215566", "marketing_category": "ANDA", "marketing_start_date": "20220922", "listing_expiration_date": "20261231"}