Package 68071-3816-1

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3816-1
Digits Only 6807138161
Product NDC 68071-3816
Product ID 68071-3816_312da1f3-1909-cc1d-e063-6394a90adc5e
Description

1000 TABLET in 1 BOTTLE, PLASTIC (68071-3816-1)

Marketing

Marketing Status
Marketed Since 2025-03-25
Brand phentermine hydrochloride
Generic phentermine hydrochloride
Sample Package No

Linked Drug Pages (1)

Phentermine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "312da1f3-1909-cc1d-e063-6394a90adc5e", "openfda": {"upc": ["0368071381610"], "unii": ["0K2I505OTV"], "spl_set_id": ["312d9742-6a65-c1cb-e063-6394a90a2e66"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (68071-3816-1)", "package_ndc": "68071-3816-1", "marketing_start_date": "20250325"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68071-3816_312da1f3-1909-cc1d-e063-6394a90adc5e", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3816", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA040526", "marketing_category": "ANDA", "marketing_start_date": "20130812", "listing_expiration_date": "20261231"}