Package 57664-606-88

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-606-88
Digits Only 5766460688
Product NDC 57664-606
Product ID 57664-606_0da4b745-d498-8823-e063-6394a90a4524
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-606-88)

Marketing

Marketing Status
Marketed Since 2020-08-20
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": "0da4b745-d498-8823-e063-6394a90a4524", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["d048e52d-7406-4fc1-9a72-c073bafc7439"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-606-88)", "package_ndc": "57664-606-88", "marketing_start_date": "20200820"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "57664-606_0da4b745-d498-8823-e063-6394a90a4524", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-606", "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": "18 mg/1"}], "application_number": "ANDA205135", "marketing_category": "ANDA", "marketing_start_date": "20200820", "listing_expiration_date": "20261231"}