Package 43386-571-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43386-571-01
Digits Only 4338657101
Product NDC 43386-571
Product ID 43386-571_c9e22f02-1ba0-41b6-ad52-181d18094553
Description

100 TABLET, CHEWABLE in 1 BOTTLE (43386-571-01)

Marketing

Marketing Status
Marketed Since 2015-04-06
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": "c9e22f02-1ba0-41b6-ad52-181d18094553", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091152", "1091322", "1091389"], "spl_set_id": ["5bfe50ed-171f-4c40-bc0b-20c68e8e2025"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (43386-571-01)", "package_ndc": "43386-571-01", "marketing_start_date": "20150406"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "43386-571_c9e22f02-1ba0-41b6-ad52-181d18094553", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43386-571", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA204115", "marketing_category": "ANDA", "marketing_start_date": "20150406", "listing_expiration_date": "20261231"}