Package 62037-725-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62037-725-01
Digits Only 6203772501
Product NDC 62037-725
Product ID 62037-725_7f865b23-e348-4b4a-84e1-5031dbd2cb4f
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-725-01)

Marketing

Marketing Status
Marketed Since 2019-03-04
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": "7f865b23-e348-4b4a-84e1-5031dbd2cb4f", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["85ef422d-af27-4126-9841-6892af1871d6"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-725-01)", "package_ndc": "62037-725-01", "marketing_start_date": "20190304"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "62037-725_7f865b23-e348-4b4a-84e1-5031dbd2cb4f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "62037-725", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "18 mg/1"}], "application_number": "ANDA076772", "marketing_category": "ANDA", "marketing_start_date": "20190304", "listing_expiration_date": "20261231"}