Package 71335-1312-1

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1312-1
Digits Only 7133513121
Product NDC 71335-1312
Product ID 71335-1312_0f091a47-c71c-0d97-e063-6394a90a50bf
Description

30 TABLET in 1 BOTTLE (71335-1312-1)

Marketing

Marketing Status
Marketed Since 2019-08-22
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": "0f091a47-c71c-0d97-e063-6394a90a50bf", "openfda": {"unii": ["0K2I505OTV"], "spl_set_id": ["95f908c2-1003-4e8f-8e4a-86f493456878"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1312-1)", "package_ndc": "71335-1312-1", "marketing_start_date": "20190822"}], "brand_name": "Phentermine Hydrochloride", "product_id": "71335-1312_0f091a47-c71c-0d97-e063-6394a90a50bf", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "71335-1312", "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": "20130812", "listing_expiration_date": "20261231"}