Package 67877-602-91

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67877-602-91
Digits Only 6787760291
Product NDC 67877-602
Product ID 67877-602_2a496565-0f45-49a8-b49b-e4a734aee439
Description

500 mL in 1 BOTTLE (67877-602-91)

Marketing

Marketing Status
Marketed Since 2020-04-01
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": "2a496565-0f45-49a8-b49b-e4a734aee439", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["5fa3da25-13aa-4ee3-acf5-cd505f4688d0"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (67877-602-91)", "package_ndc": "67877-602-91", "marketing_start_date": "20200401"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "67877-602_2a496565-0f45-49a8-b49b-e4a734aee439", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "67877-602", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA211647", "marketing_category": "ANDA", "marketing_start_date": "20200401", "listing_expiration_date": "20261231"}