Package 63629-1107-1

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1107-1
Digits Only 6362911071
Product NDC 63629-1107
Product ID 63629-1107_fc628475-40f6-4c86-be0b-1df0d41f470c
Description

1000 TABLET in 1 BOTTLE, PLASTIC (63629-1107-1)

Marketing

Marketing Status
Marketed Since 2020-06-17
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": "fc628475-40f6-4c86-be0b-1df0d41f470c", "openfda": {"unii": ["0K2I505OTV"], "spl_set_id": ["0ca26b58-0a93-4a10-be4d-63a4ad5eecf8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (63629-1107-1)", "package_ndc": "63629-1107-1", "marketing_start_date": "20200617"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63629-1107_fc628475-40f6-4c86-be0b-1df0d41f470c", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63629-1107", "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": "30 mg/1"}], "application_number": "ANDA040526", "marketing_category": "ANDA", "marketing_start_date": "20200617", "listing_expiration_date": "20261231"}