Package 43602-177-05

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43602-177-05
Digits Only 4360217705
Product NDC 43602-177
Description

500 mL in 1 BOTTLE (43602-177-05)

Marketing

Marketing Status
Marketed Since 2021-01-29
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": "eadd6980-7aad-464b-9ce8-cf7b1a20064d", "openfda": {"nui": ["N0000175739", "N0000175729"], "upc": ["0343602178259", "0343602177252"], "unii": ["207ZZ9QZ49"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["45ebb59c-9603-4df6-b1be-3295ba2db1e7"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]"], "manufacturer_name": ["Ascent Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (43602-177-05)", "package_ndc": "43602-177-05", "marketing_start_date": "20210129"}, {"sample": false, "description": "250 mL in 1 BOTTLE (43602-177-25)", "package_ndc": "43602-177-25", "marketing_start_date": "20210129"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "43602-177_eadd6980-7aad-464b-9ce8-cf7b1a20064d", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43602-177", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Ascent Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE", "strength": "5 mg/5mL"}], "application_number": "ANDA207417", "marketing_category": "ANDA", "marketing_start_date": "20210129", "listing_expiration_date": "20261231"}