Package 43386-573-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43386-573-01
Digits Only 4338657301
Product NDC 43386-573
Product ID 43386-573_ac26e6b6-2be0-458d-8acc-d963bcca13a5
Description

100 TABLET in 1 BOTTLE (43386-573-01)

Marketing

Marketing Status
Marketed Since 2016-01-20
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": "ac26e6b6-2be0-458d-8acc-d963bcca13a5", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["ec8a8896-077d-4dee-9e10-97172512c5ed"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-573-01)", "package_ndc": "43386-573-01", "marketing_start_date": "20160120"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "43386-573_ac26e6b6-2be0-458d-8acc-d963bcca13a5", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43386-573", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207884", "marketing_category": "ANDA", "marketing_start_date": "20160120", "listing_expiration_date": "20261231"}