Package 72162-2573-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2573-1
Digits Only 7216225731
Product NDC 72162-2573
Product ID 72162-2573_f90931ea-7429-4597-b094-484b5ef86d0d
Description

100 CAPSULE in 1 BOTTLE (72162-2573-1)

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": "f90931ea-7429-4597-b094-484b5ef86d0d", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197985"], "spl_set_id": ["093ff3c7-3ecc-47b4-9ae6-5218bcd262b2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2573-1)", "package_ndc": "72162-2573-1", "marketing_start_date": "20251117"}], "brand_name": "Minocycline Hydrochloride", "product_id": "72162-2573_f90931ea-7429-4597-b094-484b5ef86d0d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-2573", "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": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}