Package 70752-131-14

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70752-131-14
Digits Only 7075213114
Product NDC 70752-131
Product ID 70752-131_80b36f9d-4d27-46af-837b-70d2daec0dba
Description

500 mL in 1 BOTTLE, PLASTIC (70752-131-14)

Marketing

Marketing Status
Marketed Since 2020-06-04
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": "80b36f9d-4d27-46af-837b-70d2daec0dba", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["59de488c-c3f8-415d-9e9f-9102c090aac8"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (70752-131-14)", "package_ndc": "70752-131-14", "marketing_start_date": "20200604"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "70752-131_80b36f9d-4d27-46af-837b-70d2daec0dba", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "70752-131", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA213567", "marketing_category": "ANDA", "marketing_start_date": "20200604", "listing_expiration_date": "20261231"}