Package 62175-312-37

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62175-312-37
Digits Only 6217531237
Product NDC 62175-312
Product ID 62175-312_9509caaf-43ee-4742-85f6-0fecbc9f8c0c
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-312-37)

Marketing

Marketing Status
Marketed Since 2013-09-23
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": "9509caaf-43ee-4742-85f6-0fecbc9f8c0c", "openfda": {"upc": ["0362175312372", "0362175311375"], "unii": ["4B3SC438HI"], "rxcui": ["2001564", "2001565", "2001566", "2001568"], "spl_set_id": ["3d1f5aff-5d39-496c-b5ed-7f3c70ec641c"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-312-37)", "package_ndc": "62175-312-37", "marketing_start_date": "20130923"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "62175-312_9509caaf-43ee-4742-85f6-0fecbc9f8c0c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "62175-312", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "36 mg/1"}], "application_number": "ANDA091695", "marketing_category": "ANDA", "marketing_start_date": "20130923", "listing_expiration_date": "20271231"}