Package 70518-1752-1

Brand: chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1752-1
Digits Only 7051817521
Product NDC 70518-1752
Product ID 70518-1752_49651fec-b19d-b9cb-e063-6394a90a83fd
Description

30 CAPSULE in 1 BLISTER PACK (70518-1752-1)

Marketing

Marketing Status
Marketed Since 2021-12-10
Brand chlordiazepoxide hydrochloride
Generic chlordiazepoxide hydrochloride
Sample Package No

Linked Drug Pages (1)

Chlordiazepoxide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49651fec-b19d-b9cb-e063-6394a90a83fd", "openfda": {"unii": ["MFM6K1XWDK"], "rxcui": ["905369"], "spl_set_id": ["9aba3135-00ff-47ba-b926-55eb16b361bf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1752-1)", "package_ndc": "70518-1752-1", "marketing_start_date": "20211210"}], "brand_name": "Chlordiazepoxide Hydrochloride", "product_id": "70518-1752_49651fec-b19d-b9cb-e063-6394a90a83fd", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-1752", "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": "10 mg/1"}], "application_number": "ANDA083116", "marketing_category": "ANDA", "marketing_start_date": "20181227", "listing_expiration_date": "20271231"}