clorazepate dipotassium
Generic: clorazepate dipotassium
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
clorazepate dipotassium
Generic Name
clorazepate dipotassium
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
clorazepate dipotassium 15 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622100
Hyphenated Format
72162-2100
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72162-2100-1)
Packages (1)
Ingredients (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"}