Package 10702-108-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-108-01
Digits Only 1070210801
Product NDC 10702-108
Product ID 10702-108_445dff50-b3a4-8602-e063-6294a90aef3b
Description

100 TABLET in 1 BOTTLE (10702-108-01)

Marketing

Marketing Status
Marketed Since 2015-12-04
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "445dff50-b3a4-8602-e063-6294a90aef3b", "openfda": {"upc": ["0310702108011", "0310702106017", "0310702107014"], "unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["0c717ae4-ec27-47db-ac1b-e504dbb379be"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-108-01)", "package_ndc": "10702-108-01", "marketing_start_date": "20151204"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "10702-108_445dff50-b3a4-8602-e063-6294a90aef3b", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-108", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "KVK-TECH, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA206931", "marketing_category": "ANDA", "marketing_start_date": "20151204", "listing_expiration_date": "20261231"}