Package 63629-2477-1
Brand: phentermine hydrochloride
Generic: phentermine hydrochloridePackage Facts
Identity
Package NDC
63629-2477-1
Digits Only
6362924771
Product NDC
63629-2477
Description
100 TABLET in 1 BOTTLE (63629-2477-1)
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": "8e20148c-7992-4efa-81a0-867934c216ff", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["328d6a39-34f4-4b74-a1bf-6ec6005b1322"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2477-1)", "package_ndc": "63629-2477-1", "marketing_start_date": "20210308"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63629-2477_8e20148c-7992-4efa-81a0-867934c216ff", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63629-2477", "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": "ANDA200272", "marketing_category": "ANDA", "marketing_start_date": "20110308", "listing_expiration_date": "20261231"}