Package 71930-025-52

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71930-025-52
Digits Only 7193002552
Product NDC 71930-025
Product ID 71930-025_2ec047c6-e9ea-4093-bb03-1b3f80fb2a13
Description

500 mL in 1 BOTTLE (71930-025-52)

Marketing

Marketing Status
Marketed Since 2019-03-29
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": "2ec047c6-e9ea-4093-bb03-1b3f80fb2a13", "openfda": {"upc": ["0371930025525"], "unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["298fb86d-7d94-49e1-b743-3e7801122422"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (71930-025-52)", "package_ndc": "71930-025-52", "marketing_start_date": "20190329"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "71930-025_2ec047c6-e9ea-4093-bb03-1b3f80fb2a13", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "71930-025", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA210139", "marketing_category": "ANDA", "marketing_start_date": "20190329", "listing_expiration_date": "20261231"}