Package 70518-4565-0

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4565-0
Digits Only 7051845650
Product NDC 70518-4565
Product ID 70518-4565_49ff6a70-4d73-b34a-e063-6394a90a338d
Description

28 CAPSULE in 1 BOTTLE, PLASTIC (70518-4565-0)

Marketing

Marketing Status
Marketed Since 2026-02-03
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": "49ff6a70-4d73-b34a-e063-6394a90a338d", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["6597bdc9-9e3a-4c11-8b39-27b47f863287"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (70518-4565-0)", "package_ndc": "70518-4565-0", "marketing_start_date": "20260203"}], "brand_name": "Minocycline Hydrochloride", "product_id": "70518-4565_49ff6a70-4d73-b34a-e063-6394a90a338d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-4565", "generic_name": "Minocycline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA063065", "marketing_category": "ANDA", "marketing_start_date": "20260203", "listing_expiration_date": "20271231"}