Package 70518-0157-0

Brand: chlordiazepoxide hydrochloride

Generic: chlordiazepoxide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-0157-0
Digits Only 7051801570
Product NDC 70518-0157
Product ID 70518-0157_47e36f24-0c8e-d4b3-e063-6294a90a97e9
Description

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

Marketing

Marketing Status
Marketed Since 2017-01-19
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": "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"}