Package 42806-563-01

Brand: chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-563-01
Digits Only 4280656301
Product NDC 42806-563
Description

100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-563-01)

Marketing

Marketing Status
Marketed Since 2021-05-11
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": "eab706f9-1c3b-4be4-a118-4cfd55ce2c11", "openfda": {"upc": ["0342806563014", "0342806562017", "0342806561010"], "unii": ["MFM6K1XWDK"], "spl_set_id": ["8255992f-3256-4558-bd0d-cfe350d95f25"], "manufacturer_name": ["Epic Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-563-01)", "package_ndc": "42806-563-01", "marketing_start_date": "20210511"}], "brand_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "product_id": "42806-563_eab706f9-1c3b-4be4-a118-4cfd55ce2c11", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "42806-563", "dea_schedule": "CIV", "generic_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "labeler_name": "Epic Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORDIAZEPOXIDE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA085475", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}