Package 10702-164-50

Brand: methylphenidate

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-164-50
Digits Only 1070216450
Product NDC 10702-164
Product ID 10702-164_445ee0dc-ce64-e21a-e063-6294a90ac320
Description

500 mL in 1 BOTTLE (10702-164-50)

Marketing

Marketing Status
Marketed Since 2017-01-23
Brand methylphenidate
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "445ee0dc-ce64-e21a-e063-6294a90ac320", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["2cf1b26b-199d-4c7f-ab64-4805a9def2cc"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (10702-164-50)", "package_ndc": "10702-164-50", "marketing_start_date": "20170123"}], "brand_name": "Methylphenidate", "product_id": "10702-164_445ee0dc-ce64-e21a-e063-6294a90ac320", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-164", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA207485", "marketing_category": "ANDA", "marketing_start_date": "20170123", "listing_expiration_date": "20261231"}