Package 76420-108-30

Brand: phentermine hydrochloride

Generic: phentermine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-108-30
Digits Only 7642010830
Product NDC 76420-108
Product ID 76420-108_b2ddcdd0-7292-99df-e053-2a95a90a8818
Description

30 TABLET in 1 BOTTLE (76420-108-30)

Marketing

Marketing Status
Marketed Since 2020-10-30
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": "b2ddcdd0-7292-99df-e053-2a95a90a8818", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["de76ed27-ac43-4923-b73f-461d33941f6b"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-108-30)", "package_ndc": "76420-108-30", "marketing_start_date": "20201030"}], "brand_name": "Phentermine hydrochloride", "product_id": "76420-108_b2ddcdd0-7292-99df-e053-2a95a90a8818", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "76420-108", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA205008", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}