Package 68071-3808-1
Brand: phentermine hydrochloride
Generic: phentermine hydrochloridePackage Facts
Identity
Package NDC
68071-3808-1
Digits Only
6807138081
Product NDC
68071-3808
Description
100 TABLET in 1 BOTTLE (68071-3808-1)
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": "30b471d8-c5ab-9007-e063-6394a90ac8e9", "openfda": {"upc": ["0368071380811"], "unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["30b48126-45f3-21fa-e063-6294a90a968f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3808-1)", "package_ndc": "68071-3808-1", "marketing_start_date": "20250319"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68071-3808_30b471d8-c5ab-9007-e063-6394a90ac8e9", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3808", "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": "37.5 mg/1"}], "application_number": "ANDA200272", "marketing_category": "ANDA", "marketing_start_date": "20110308", "listing_expiration_date": "20261231"}