Package 72789-525-30

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-525-30
Digits Only 7278952530
Product NDC 72789-525
Product ID 72789-525_3e74d98b-05cb-180f-e063-6294a90ac0b5
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-525-30)

Marketing

Marketing Status
Marketed Since 2025-09-10
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": "3e74d98b-05cb-180f-e063-6294a90ac0b5", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629699"], "spl_set_id": ["3e74e8a3-2670-97f5-e063-6394a90a361e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-525-30)", "package_ndc": "72789-525-30", "marketing_start_date": "20250910"}], "brand_name": "Minocycline Hydrochloride", "product_id": "72789-525_3e74d98b-05cb-180f-e063-6294a90ac0b5", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72789-525", "generic_name": "Minocycline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}