Package 70518-4510-0

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 70518-4510-0
Digits Only 7051845100
Product NDC 70518-4510
Product ID 70518-4510_41e80156-4121-31e8-e063-6394a90a8ebd
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4510-0)

Marketing

Marketing Status
Marketed Since 2025-10-24
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41e80156-4121-31e8-e063-6394a90a8ebd", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["051654c7-8ba6-44f2-842c-72f515e9b32d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4510-0)", "package_ndc": "70518-4510-0", "marketing_start_date": "20251024"}], "brand_name": "Doxycycline Hyclate", "product_id": "70518-4510_41e80156-4121-31e8-e063-6394a90a8ebd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-4510", "generic_name": "Doxycycline Hyclate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20251024", "listing_expiration_date": "20261231"}