Package 53489-676-07

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53489-676-07
Digits Only 5348967607
Product NDC 53489-676
Description

30 TABLET in 1 BOTTLE, PLASTIC (53489-676-07)

Marketing

Marketing Status
Marketed Since 2013-08-12
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": "39e24c57-7266-2bf6-e063-6294a90afdd1", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["02b8f684-b1ca-4ab7-9567-bcacc6a92779"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (53489-676-01)", "package_ndc": "53489-676-01", "marketing_start_date": "20130812"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE, PLASTIC (53489-676-03)", "package_ndc": "53489-676-03", "marketing_start_date": "20130812"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (53489-676-05)", "package_ndc": "53489-676-05", "marketing_start_date": "20130812"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (53489-676-06)", "package_ndc": "53489-676-06", "marketing_start_date": "20130812"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (53489-676-07)", "package_ndc": "53489-676-07", "marketing_start_date": "20130812"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (53489-676-10)", "package_ndc": "53489-676-10", "marketing_start_date": "20130812"}], "brand_name": "Phentermine Hydrochloride", "product_id": "53489-676_39e24c57-7266-2bf6-e063-6294a90afdd1", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "53489-676", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA040526", "marketing_category": "ANDA", "marketing_start_date": "20130812", "listing_expiration_date": "20261231"}