Package 59651-339-50

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-339-50
Digits Only 5965133950
Product NDC 59651-339
Product ID 59651-339_2ef3b8ae-dd97-473f-bd81-c8c1b192c0ed
Description

50 TABLET, FILM COATED in 1 CONTAINER (59651-339-50)

Marketing

Marketing Status
Marketed Since 2020-05-01
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": "2ef3b8ae-dd97-473f-bd81-c8c1b192c0ed", "openfda": {"unii": ["0020414E5U"], "rxcui": ["207362", "207364", "403840"], "spl_set_id": ["799a9871-3249-471e-b88d-5d8f7d4b96ad"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 CONTAINER (59651-339-50)", "package_ndc": "59651-339-50", "marketing_start_date": "20200501"}], "brand_name": "Minocycline Hydrochloride", "product_id": "59651-339_2ef3b8ae-dd97-473f-bd81-c8c1b192c0ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "59651-339", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA213662", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}