Package 60687-807-01

Brand: chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-807-01
Digits Only 6068780701
Product NDC 60687-807
Description

100 BLISTER PACK in 1 CARTON (60687-807-01) / 1 CAPSULE in 1 BLISTER PACK (60687-807-11)

Marketing

Marketing Status
Marketed Since 2024-07-03
Brand chlordiazepoxide hydrochloride
Generic chlordiazepoxide hydrochloride
Sample Package No

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"}