Package 10702-040-01

Brand: benzphetamine hydrochloride

Generic: benzphetamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-040-01
Digits Only 1070204001
Product NDC 10702-040
Description

100 TABLET in 1 BOTTLE (10702-040-01)

Marketing

Marketing Status
Marketed Since 2010-07-21
Brand benzphetamine hydrochloride
Generic benzphetamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15d75638-8ac7-e610-e063-6394a90af99c", "openfda": {"unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["14d4589d-7f1c-4b6e-9557-59dad39b0960"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-040-01)", "package_ndc": "10702-040-01", "marketing_start_date": "20100721"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-040-03)", "package_ndc": "10702-040-03", "marketing_start_date": "20100721"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-040-10)", "package_ndc": "10702-040-10", "marketing_start_date": "20100721"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-040-50)", "package_ndc": "10702-040-50", "marketing_start_date": "20100721"}], "brand_name": "BENZPHETAMINE HYDROCHLORIDE", "product_id": "10702-040_15d75638-8ac7-e610-e063-6394a90af99c", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-040", "dea_schedule": "CIII", "generic_name": "benzphetamine hydrochloride", "labeler_name": "KVK-TECH, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZPHETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "BENZPHETAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090968", "marketing_category": "ANDA", "marketing_start_date": "20100721", "listing_expiration_date": "20261231"}