chlordiazepoxide hydrochloride
Generic: chlordiazepoxide hydrochloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
chlordiazepoxide hydrochloride
Generic Name
chlordiazepoxide hydrochloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
chlordiazepoxide hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5171
Product ID
68071-5171_1b567b38-ffc3-11d0-e063-6394a90a6c7d
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715171
Hyphenated Format
68071-5171
Supplemental Identifiers
RxCUI
UPC
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
- 30 CAPSULE in 1 BOTTLE (68071-5171-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b567b38-ffc3-11d0-e063-6394a90a6c7d", "openfda": {"upc": ["0368071517132"], "unii": ["MFM6K1XWDK"], "rxcui": ["905495"], "spl_set_id": ["9e64d2d8-b12c-5639-e053-2a95a90aab80"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-5171-3)", "package_ndc": "68071-5171-3", "marketing_start_date": "20200212"}], "brand_name": "Chlordiazepoxide Hydrochloride", "product_id": "68071-5171_1b567b38-ffc3-11d0-e063-6394a90a6c7d", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68071-5171", "dea_schedule": "CIV", "generic_name": "Chlordiazepoxide Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,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"}