Package 71335-2296-1

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2296-1
Digits Only 7133522961
Product NDC 71335-2296
Description

100 CAPSULE in 1 BOTTLE (71335-2296-1)

Marketing

Marketing Status
Marketed Since 2025-01-31
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": "e3949592-b026-44fe-83c9-0371a6db5adc", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803348"], "spl_set_id": ["70f68311-8d1f-4b8e-b8a7-13bc4c17727e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-2296-1)", "package_ndc": "71335-2296-1", "marketing_start_date": "20250131"}], "brand_name": "Phentermine hydrochloride", "product_id": "71335-2296_e3949592-b026-44fe-83c9-0371a6db5adc", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "71335-2296", "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": "ANDA205017", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}