Package 0591-3891-19

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-3891-19
Digits Only 0591389119
Product NDC 0591-3891
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3891-19)

Marketing

Marketing Status
Marketed Since 2020-09-30
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1895894a-ed70-4f82-b512-6bc184ee806c", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1648183", "1806200", "1806202", "1806204", "1806206", "1806208", "1806210"], "spl_set_id": ["ecbb4a30-21ac-42e1-b4e9-6c35344ffc45"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3891-19)", "package_ndc": "0591-3891-19", "marketing_start_date": "20200930"}], "brand_name": "methylphenidate hydrochloride", "product_id": "0591-3891_1895894a-ed70-4f82-b512-6bc184ee806c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0591-3891", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methylphenidate hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208861", "marketing_category": "ANDA", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}