Package 72865-123-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72865-123-01
Digits Only 7286512301
Product NDC 72865-123
Description

100 TABLET in 1 BOTTLE (72865-123-01)

Marketing

Marketing Status
Marketed Since 2020-02-26
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a38c200-2e90-42b8-97e8-e5b64a7078e0", "openfda": {"upc": ["0372865124017", "0372865123010", "0372865122013"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["94dc74d4-b4ef-45bc-b502-54ec692e9bd5"], "manufacturer_name": ["XLCare Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-123-01)", "package_ndc": "72865-123-01", "marketing_start_date": "20200226"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-123-05)", "package_ndc": "72865-123-05", "marketing_start_date": "20200226"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72865-123_0a38c200-2e90-42b8-97e8-e5b64a7078e0", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72865-123", "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": "10 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20200226", "listing_expiration_date": "20261231"}