Package 72189-203-30

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-203-30
Digits Only 7218920330
Product NDC 72189-203
Product ID 72189-203_2be977e6-4cfe-9a64-e063-6294a90a9fc9
Description

30 TABLET in 1 BOTTLE (72189-203-30)

Marketing

Marketing Status
Marketed Since 2021-06-03
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": "2be977e6-4cfe-9a64-e063-6294a90a9fc9", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["c3dda0a4-b428-f3e7-e053-2995a90ad106"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-203-30)", "package_ndc": "72189-203-30", "marketing_start_date": "20210603"}], "brand_name": "PHENTERMINE HYDROCHLORIDE", "product_id": "72189-203_2be977e6-4cfe-9a64-e063-6294a90a9fc9", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72189-203", "dea_schedule": "CIV", "generic_name": "PHENTERMINE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENTERMINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA203068", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}