Package 70010-042-03

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70010-042-03
Digits Only 7001004203
Product NDC 70010-042
Product ID 70010-042_411818b5-dc2c-93c3-e063-6294a90a7638
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-042-03)

Marketing

Marketing Status
Marketed Since 2022-10-31
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": "411818b5-dc2c-93c3-e063-6294a90a7638", "openfda": {"upc": ["0370010043039", "0370010042032"], "unii": ["4B3SC438HI"], "rxcui": ["1091145", "1091225"], "spl_set_id": ["45d33807-88b2-4b42-9c86-e5b05d7adec1"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-042-01)", "package_ndc": "70010-042-01", "marketing_start_date": "20181217"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-042-03)", "package_ndc": "70010-042-03", "marketing_start_date": "20221031"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "70010-042_411818b5-dc2c-93c3-e063-6294a90a7638", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "70010-042", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA210992", "marketing_category": "ANDA", "marketing_start_date": "20181217", "listing_expiration_date": "20261231"}