Package 72162-1229-0

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1229-0
Digits Only 7216212290
Product NDC 72162-1229
Description

1000 TABLET in 1 BOTTLE (72162-1229-0)

Marketing

Marketing Status
Marketed Since 2023-04-21
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": "c8735cfd-5bbb-465c-ad8b-28627352fb4d", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["50efa498-11c5-41fa-95ac-419fcc10da03"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1229-0)", "package_ndc": "72162-1229-0", "marketing_start_date": "20230421"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1229-1)", "package_ndc": "72162-1229-1", "marketing_start_date": "20230421"}], "brand_name": "Phentermine hydrochloride", "product_id": "72162-1229_c8735cfd-5bbb-465c-ad8b-28627352fb4d", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72162-1229", "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"}