Package 66267-394-60
Brand: phendimetrazine tartrate
Generic: phendimetrazine tartratePackage Facts
Identity
Package NDC
66267-394-60
Digits Only
6626739460
Product NDC
66267-394
Description
60 TABLET in 1 BOTTLE (66267-394-60)
Marketing
Marketing Status
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": "1fa6afe6-d924-02d3-e063-6394a90a41c7", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["40e5b0bf-347e-30f6-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc,"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (66267-394-60)", "package_ndc": "66267-394-60", "marketing_start_date": "20161109"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "66267-394_1fa6afe6-d924-02d3-e063-6394a90a41c7", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "66267-394", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "NuCare Pharmaceuticals, Inc,", "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": "20261231"}