Package 13811-700-30

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13811-700-30
Digits Only 1381170030
Product NDC 13811-700
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-700-30)

Marketing

Marketing Status
Marketed Since 2022-06-23
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": "ba649db4-df0d-4587-8370-3f866e66e54b", "openfda": {"upc": ["0313811700305", "0313811711301"], "unii": ["4B3SC438HI"], "rxcui": ["2605796", "2605798"], "spl_set_id": ["dd8d7b6e-c23d-4e16-bb53-959e9127ebc6"], "manufacturer_name": ["Trigen Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-700-30)", "package_ndc": "13811-700-30", "marketing_start_date": "20220623"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "13811-700_ba649db4-df0d-4587-8370-3f866e66e54b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "13811-700", "dea_schedule": "CII", "generic_name": "Methylphenidate hydrochloride", "labeler_name": "Trigen Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "63 mg/1"}], "application_number": "NDA216117", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220623", "listing_expiration_date": "20261231"}