Package 70518-4544-0

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 70518-4544-0
Digits Only 7051845440
Product NDC 70518-4544
Description

20 TABLET in 1 BOTTLE, PLASTIC (70518-4544-0)

Marketing

Marketing Status
Marketed Since 2026-01-11
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4830c8b3-40c3-3cef-e063-6394a90acaf2", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["d421b771-de88-4769-949f-8a24baa69c25"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-4544-0)", "package_ndc": "70518-4544-0", "marketing_start_date": "20260111"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "70518-4544_4830c8b3-40c3-3cef-e063-6394a90acaf2", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-4544", "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": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20260111", "listing_expiration_date": "20271231"}