Package 66758-275-01

Brand: ritalin

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66758-275-01
Digits Only 6675827501
Product NDC 66758-275
Product ID 66758-275_3cf2c541-a65c-4651-ab30-3451a5581f8f
Description

100 TABLET in 1 BOTTLE (66758-275-01)

Marketing

Marketing Status
Marketed Since 2024-12-18
Brand ritalin
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Ritalin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cf2c541-a65c-4651-ab30-3451a5581f8f", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091379", "1091392", "1091395", "1091497", "1091500"], "spl_set_id": ["d6fb2750-cdab-4749-ba0d-7534840a5892"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66758-275-01)", "package_ndc": "66758-275-01", "marketing_start_date": "20241218"}], "brand_name": "Ritalin", "product_id": "66758-275_3cf2c541-a65c-4651-ab30-3451a5581f8f", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "66758-275", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ritalin", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA010187", "marketing_category": "NDA", "marketing_start_date": "19551231", "listing_expiration_date": "20261231"}