Package 43386-862-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43386-862-01
Digits Only 4338686201
Product NDC 43386-862
Product ID 43386-862_4d2d72fd-412e-4556-9adc-d4673576a29c
Description

100 TABLET in 1 BOTTLE (43386-862-01)

Marketing

Marketing Status
Marketed Since 2015-12-04
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4d2d72fd-412e-4556-9adc-d4673576a29c", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["a61932ef-c2b6-4363-a21d-1f0358f317b6"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-862-01)", "package_ndc": "43386-862-01", "marketing_start_date": "20151204"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "43386-862_4d2d72fd-412e-4556-9adc-d4673576a29c", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43386-862", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA204534", "marketing_category": "ANDA", "marketing_start_date": "20151204", "listing_expiration_date": "20261231"}