Package 72865-134-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72865-134-01
Digits Only 7286513401
Product NDC 72865-134
Product ID 72865-134_f0d4af9c-1d16-4405-ac11-6c412af320eb
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-134-01)

Marketing

Marketing Status
Marketed Since 2020-02-24
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": "f0d4af9c-1d16-4405-ac11-6c412af320eb", "openfda": {"upc": ["0372865133019", "0372865135013", "0372865136010", "0372865134016"], "unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["b07150db-fd99-4400-bb83-b3a7544a917a"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-134-01)", "package_ndc": "72865-134-01", "marketing_start_date": "20200224"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "72865-134_f0d4af9c-1d16-4405-ac11-6c412af320eb", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72865-134", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "27 mg/1"}], "application_number": "ANDA211009", "marketing_category": "ANDA", "marketing_start_date": "20200224", "listing_expiration_date": "20261231"}