Package 53489-647-06

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 53489-647-06
Digits Only 5348964706
Product NDC 53489-647
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06)

Marketing

Marketing Status
Marketed Since 2005-05-13
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": "31dd6775-5a9a-9e21-e063-6294a90aa546", "openfda": {"upc": ["0353489647014"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["bff3f426-44fc-4dbf-96df-df44011103e8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01)", "package_ndc": "53489-647-01", "marketing_start_date": "20050513"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03)", "package_ndc": "53489-647-03", "marketing_start_date": "20050513"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05)", "package_ndc": "53489-647-05", "marketing_start_date": "20050513"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06)", "package_ndc": "53489-647-06", "marketing_start_date": "20050513"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)", "package_ndc": "53489-647-07", "marketing_start_date": "20050513"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10)", "package_ndc": "53489-647-10", "marketing_start_date": "20050513"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90)", "package_ndc": "53489-647-90", "marketing_start_date": "20050513"}], "brand_name": "Doxycycline Hyclate", "product_id": "53489-647_31dd6775-5a9a-9e21-e063-6294a90aa546", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "53489-647", "generic_name": "Doxycycline Hyclate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "20 mg/1"}], "application_number": "ANDA065134", "marketing_category": "ANDA", "marketing_start_date": "20050513", "listing_expiration_date": "20261231"}