Package 13107-381-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13107-381-01
Digits Only 1310738101
Product NDC 13107-381
Product ID 13107-381_f821bfff-5013-4850-8e10-33e5c146df4a
Description

100 TABLET in 1 BOTTLE (13107-381-01)

Marketing

Marketing Status
Marketed Since 2017-04-11
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": "f821bfff-5013-4850-8e10-33e5c146df4a", "openfda": {"upc": ["0313107381010", "0313107382017", "0313107380013"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["35be77db-fbe3-487e-a220-a08a11aaec28"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-381-01)", "package_ndc": "13107-381-01", "marketing_start_date": "20170411"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "13107-381_f821bfff-5013-4850-8e10-33e5c146df4a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "13107-381", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209276", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}