Package 71335-2297-2
Brand: phentermine hydrochloride
Generic: phentermine hydrochloridePackage Facts
Identity
Package NDC
71335-2297-2
Digits Only
7133522972
Product NDC
71335-2297
Description
100 TABLET in 1 BOTTLE (71335-2297-2)
Marketing
Marketing Status
Brand
phentermine hydrochloride
Generic
phentermine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37328161-b71b-4ed2-9708-baaf19693bc2", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["e08b4f49-de9f-490d-b11d-d865439f5fad"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2297-1)", "package_ndc": "71335-2297-1", "marketing_start_date": "20250131"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2297-2)", "package_ndc": "71335-2297-2", "marketing_start_date": "20250131"}], "brand_name": "Phentermine hydrochloride", "product_id": "71335-2297_37328161-b71b-4ed2-9708-baaf19693bc2", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "71335-2297", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA205008", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}