Package 72189-253-30

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-253-30
Digits Only 7218925330
Product NDC 72189-253
Description

30 CAPSULE in 1 BOTTLE (72189-253-30)

Marketing

Marketing Status
Marketed Since 2021-08-25
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": "2c28de82-39db-9df3-e063-6394a90ac7f9", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["ca683656-16a6-9602-e053-2a95a90aa895"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-253-30)", "package_ndc": "72189-253-30", "marketing_start_date": "20210825"}], "brand_name": "PHENTERMINE HYDROCHLORIDE", "product_id": "72189-253_2c28de82-39db-9df3-e063-6394a90ac7f9", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72189-253", "dea_schedule": "CIV", "generic_name": "PHENTERMINE HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENTERMINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA205019", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}