Package 31722-953-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-953-01
Digits Only 3172295301
Product NDC 31722-953
Product ID 31722-953_1d1d77b9-0f73-4daf-8ca6-0837caa03bac
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-953-01)

Marketing

Marketing Status
Marketed Since 2019-09-03
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": "1d1d77b9-0f73-4daf-8ca6-0837caa03bac", "openfda": {"upc": ["0331722955010", "0331722954013", "0331722952019", "0331722953016"], "unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["b9af3104-172d-4975-9301-b9fe7db9ef12"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-953-01)", "package_ndc": "31722-953-01", "marketing_start_date": "20190903"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "31722-953_1d1d77b9-0f73-4daf-8ca6-0837caa03bac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "31722-953", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "27 mg/1"}], "application_number": "ANDA211009", "marketing_category": "ANDA", "marketing_start_date": "20190903", "listing_expiration_date": "20261231"}