Package 72162-2575-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2575-1
Digits Only 7216225751
Product NDC 72162-2575
Product ID 72162-2575_38b73048-9d52-416c-a03b-87ea29384df3
Description

100 TABLET in 1 BOTTLE (72162-2575-1)

Marketing

Marketing Status
Marketed Since 2025-11-17
Brand minocycline hydrochloride
Generic minocycline hydrochloride
Sample Package No

Linked Drug Pages (1)

MINOCYCLINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38b73048-9d52-416c-a03b-87ea29384df3", "openfda": {"unii": ["0020414E5U"], "rxcui": ["207362"], "spl_set_id": ["bae17358-1180-4ca8-b163-f9a6f4f83a3d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2575-1)", "package_ndc": "72162-2575-1", "marketing_start_date": "20251117"}], "brand_name": "MINOCYCLINE HYDROCHLORIDE", "product_id": "72162-2575_38b73048-9d52-416c-a03b-87ea29384df3", "dosage_form": "TABLET", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-2575", "generic_name": "MINOCYCLINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOCYCLINE HYDROCHLORIDE", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA065156", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}