Package 50090-2235-2

Brand: phendimetrazine tartrate

Generic: phendimetrazine tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-2235-2
Digits Only 5009022352
Product NDC 50090-2235
Description

90 TABLET in 1 BOTTLE (50090-2235-2)

Marketing

Marketing Status
Marketed Since 2015-11-20
Brand phendimetrazine tartrate
Generic phendimetrazine tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d6516b2c-e14a-465c-9d5d-6aec9ef6959c", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["ef4cfd54-7d3e-4571-ae77-38ab2fd1af3d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-2235-2)", "package_ndc": "50090-2235-2", "marketing_start_date": "20151120"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "50090-2235_d6516b2c-e14a-465c-9d5d-6aec9ef6959c", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-2235", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phendimetrazine Tartrate", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "35 mg/1"}], "application_number": "ANDA091042", "marketing_category": "ANDA", "marketing_start_date": "20100915", "listing_expiration_date": "20271231"}