Package 75834-324-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 75834-324-01
Digits Only 7583432401
Product NDC 75834-324
Product ID 75834-324_4cc16009-44ad-4055-ac76-efa282f1ff47
Description

100 TABLET in 1 BOTTLE (75834-324-01)

Marketing

Marketing Status
Marketed Since 2024-04-16
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": "4cc16009-44ad-4055-ac76-efa282f1ff47", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["4cc16009-44ad-4055-ac76-efa282f1ff47"], "manufacturer_name": ["Nivagen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (75834-324-01)", "package_ndc": "75834-324-01", "marketing_start_date": "20240416"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "75834-324_4cc16009-44ad-4055-ac76-efa282f1ff47", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "75834-324", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Nivagen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208737", "marketing_category": "ANDA", "marketing_start_date": "20240416", "listing_expiration_date": "20261231"}