Package 10702-101-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-101-01
Digits Only 1070210101
Product NDC 10702-101
Product ID 10702-101_476dd35a-34a9-02dd-e063-6394a90a912a
Description

100 TABLET in 1 BOTTLE (10702-101-01)

Marketing

Marketing Status
Marketed Since 2017-05-11
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "476dd35a-34a9-02dd-e063-6394a90a912a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["1bf37f9f-29cf-4b09-9c81-eb369e35a042"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-101-01)", "package_ndc": "10702-101-01", "marketing_start_date": "20170511"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "10702-101_476dd35a-34a9-02dd-e063-6394a90a912a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-101", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA206932", "marketing_category": "ANDA", "marketing_start_date": "20170511", "listing_expiration_date": "20271231"}