Package 43547-462-12

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 43547-462-12
Digits Only 4354746212
Product NDC 43547-462
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-462-12)

Marketing

Marketing Status
Marketed Since 2018-11-28
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": "49c9be01-a1bf-48aa-8ef4-0584e8dcaac5", "openfda": {"upc": ["0343547325060", "0343547324063", "0343547462123"], "unii": ["19XTS3T51U"], "rxcui": ["799048", "1423080", "1653433"], "spl_set_id": ["0a18d4c7-9484-4d3e-b61b-e81fe63fefec"], "manufacturer_name": ["Solco Healthcare US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-462-12)", "package_ndc": "43547-462-12", "marketing_start_date": "20181128"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "43547-462_49c9be01-a1bf-48aa-8ef4-0584e8dcaac5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "43547-462", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Solco Healthcare US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA207494", "marketing_category": "ANDA", "marketing_start_date": "20181128", "listing_expiration_date": "20271231"}