chlordiazepoxide hydrochloride
Generic: chlordiazepoxide hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
chlordiazepoxide hydrochloride
Generic Name
chlordiazepoxide hydrochloride
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
chlordiazepoxide hydrochloride 25 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687807
Hyphenated Format
60687-807
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
chlordiazepoxide hydrochloride (source: ndc)
Generic Name
chlordiazepoxide hydrochloride (source: ndc)
Application Number
ANDA084769 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (60687-807-01) / 1 CAPSULE in 1 BLISTER PACK (60687-807-11)
Packages (1)
Ingredients (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"}