Package 63629-1044-1

Brand: Phentermine Hydrochloride

Generic: Phentermine Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1044-1
Digits Only 6362910441
Product NDC 63629-1044
Description

100 TABLET in 1 BOTTLE (63629-1044-1)

Marketing

Marketing Status
Marketed Since 2019-07-01
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": "fbec1189-5c39-a0e8-e053-6394a90aa02f", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["7e370e9c-b8ab-4313-85d6-2f3ccd22f7ff"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1044-1)", "package_ndc": "63629-1044-1", "marketing_start_date": "20190701"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63629-1044_fbec1189-5c39-a0e8-e053-6394a90aa02f", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63629-1044", "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"}