chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlordiazepoxide hydrochloride
Generic Name chlordiazepoxide hydrochloride
Labeler epic pharma, llc
Dosage Form CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

chlordiazepoxide hydrochloride 5 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-564
Product ID 42806-564_d7a3306e-01d4-4966-a473-62136d81f959
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085461
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2021-11-09

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806564
Hyphenated Format 42806-564

Supplemental Identifiers

RxCUI
905369 905495 905516
UPC
0342806565018 0342806566015 0342806564011
UNII
MFM6K1XWDK

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 chlordiazepoxide hydrochloride (source: ndc)
Generic Name chlordiazepoxide hydrochloride (source: ndc)
Application Number ANDA085461 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-564-01)
source: ndc

Packages (1)

42806-564-01 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-564-01)

Ingredients (1)

chlordiazepoxide hydrochloride (5 mg/1)

Linked Drug Pages (1)

CHLORDIAZEPOXIDE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d7a3306e-01d4-4966-a473-62136d81f959", "openfda": {"upc": ["0342806565018", "0342806566015", "0342806564011"], "unii": ["MFM6K1XWDK"], "rxcui": ["905369", "905495", "905516"], "spl_set_id": ["2e198c16-a929-4028-8f96-25dd23f74b10"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-564-01)", "package_ndc": "42806-564-01", "marketing_start_date": "20211109"}], "brand_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "product_id": "42806-564_d7a3306e-01d4-4966-a473-62136d81f959", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "42806-564", "dea_schedule": "CIV", "generic_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA085461", "marketing_category": "ANDA", "marketing_start_date": "20211109", "listing_expiration_date": "20261231"}