Package 63629-1045-1

Brand: Phentermine Hydrochloride

Generic: Phentermine Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1045-1
Digits Only 6362910451
Product NDC 63629-1045
Product ID 63629-1045_60d48944-39fa-4884-991a-5a3de38d100b
Description

1000 TABLET in 1 BOTTLE (63629-1045-1)

Marketing

Marketing Status
Marketed Since 2019-07-01
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": "60d48944-39fa-4884-991a-5a3de38d100b", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["a458bc67-ff80-4cb8-b718-c01e48849816"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-1045-1)", "package_ndc": "63629-1045-1", "marketing_start_date": "20190701"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63629-1045_60d48944-39fa-4884-991a-5a3de38d100b", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63629-1045", "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"}