chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlordiazepoxide hydrochloride
Generic Name chlordiazepoxide hydrochloride
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

chlordiazepoxide hydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0157
Product ID 70518-0157_47e36f24-0c8e-d4b3-e063-6294a90a97e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084769
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2017-01-19

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180157
Hyphenated Format 70518-0157

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
  • 30 CAPSULE in 1 BLISTER PACK (70518-0157-0)
source: ndc

Packages (1)

70518-0157-0 30 CAPSULE in 1 BLISTER PACK (70518-0157-0)

Ingredients (1)

chlordiazepoxide hydrochloride (25 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": "47e36f24-0c8e-d4b3-e063-6294a90a97e9", "openfda": {"unii": ["MFM6K1XWDK"], "rxcui": ["905495"], "spl_set_id": ["43daab7a-3809-4b13-b015-4806912c3c4a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0157-0)", "package_ndc": "70518-0157-0", "marketing_start_date": "20170119"}], "brand_name": "Chlordiazepoxide Hydrochloride", "product_id": "70518-0157_47e36f24-0c8e-d4b3-e063-6294a90a97e9", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-0157", "dea_schedule": "CIV", "generic_name": "Chlordiazepoxide Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20170119", "listing_expiration_date": "20271231"}