Package 57664-710-83

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-710-83
Digits Only 5766471083
Product NDC 57664-710
Product ID 57664-710_18022f9f-91bd-3d88-e063-6394a90a41f5
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83)

Marketing

Marketing Status
Marketed Since 2024-12-20
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": "18022f9f-91bd-3d88-e063-6394a90a41f5", "openfda": {"upc": ["0357664710838"], "unii": ["4B3SC438HI"], "rxcui": ["1995461"], "spl_set_id": ["18024571-4505-6d51-e063-6294a90a1972"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83)", "package_ndc": "57664-710-83", "marketing_start_date": "20241220"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88)", "package_ndc": "57664-710-88", "marketing_start_date": "20241220"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "57664-710_18022f9f-91bd-3d88-e063-6394a90a41f5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-710", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "72 mg/1"}], "application_number": "ANDA217229", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}