chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlordiazepoxide hydrochloride
Generic Name chlordiazepoxide hydrochloride
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

chlordiazepoxide hydrochloride 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-807
Product ID 60687-807_3d478726-6ce9-87a4-e063-6294a90a2958
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084769
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-07-03

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687807
Hyphenated Format 60687-807

Supplemental Identifiers

RxCUI
905495
UNII
MFM6K1XWDK

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 BLISTER PACK in 1 CARTON (60687-807-01) / 1 CAPSULE in 1 BLISTER PACK (60687-807-11)
source: ndc

Packages (1)

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": "3d478726-6ce9-87a4-e063-6294a90a2958", "openfda": {"unii": ["MFM6K1XWDK"], "rxcui": ["905495"], "spl_set_id": ["1eb5eb7a-8c5f-43a3-9b9f-6321cdb6f6c7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-807-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-807-11)", "package_ndc": "60687-807-01", "marketing_start_date": "20240703"}], "brand_name": "Chlordiazepoxide Hydrochloride", "product_id": "60687-807_3d478726-6ce9-87a4-e063-6294a90a2958", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "60687-807", "dea_schedule": "CIV", "generic_name": "Chlordiazepoxide Hydrochloride", "labeler_name": "American Health Packaging", "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": "20240703", "listing_expiration_date": "20261231"}