Package 72162-1854-3

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1854-3
Digits Only 7216218543
Product NDC 72162-1854
Product ID 72162-1854_74533915-1362-4651-89ea-3ea987b9e889
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1854-3)

Marketing

Marketing Status
Marketed Since 2024-03-11
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": "74533915-1362-4651-89ea-3ea987b9e889", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629697"], "spl_set_id": ["e1611d28-0c96-4ce2-ad5d-f62f66ec164d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1854-3)", "package_ndc": "72162-1854-3", "marketing_start_date": "20240311"}], "brand_name": "Minocycline Hydrochloride", "product_id": "72162-1854_74533915-1362-4651-89ea-3ea987b9e889", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-1854", "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": "45 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}