chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlordiazepoxide hydrochloride
Generic Name chlordiazepoxide hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

chlordiazepoxide hydrochloride 25 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-0159
Product ID 0555-0159_0e32450e-ff0c-4ab8-aeb7-34bc9fcc1962
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084769
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1976-07-01

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05550159
Hyphenated Format 0555-0159

Supplemental Identifiers

RxCUI
905369 905495 905516
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 ANDA084769 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0555-0159-02)
  • 500 CAPSULE in 1 BOTTLE (0555-0159-04)
source: ndc

Packages (2)

Ingredients (1)

chlordiazepoxide hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e32450e-ff0c-4ab8-aeb7-34bc9fcc1962", "openfda": {"unii": ["MFM6K1XWDK"], "rxcui": ["905369", "905495", "905516"], "spl_set_id": ["e3ff8641-ae8a-4016-acb1-cb1b7890f5ed"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0555-0159-02)", "package_ndc": "0555-0159-02", "marketing_start_date": "19760701"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0555-0159-04)", "package_ndc": "0555-0159-04", "marketing_start_date": "19760701"}], "brand_name": "Chlordiazepoxide Hydrochloride", "product_id": "0555-0159_0e32450e-ff0c-4ab8-aeb7-34bc9fcc1962", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0555-0159", "dea_schedule": "CIV", "generic_name": "Chlordiazepoxide Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlordiazepoxide Hydrochloride", "active_ingredients": [{"name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA084769", "marketing_category": "ANDA", "marketing_start_date": "19760701", "listing_expiration_date": "20261231"}