Package 72189-127-14

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 72189-127-14
Digits Only 7218912714
Product NDC 72189-127
Description

14 TABLET, FILM COATED in 1 BOTTLE (72189-127-14)

Marketing

Marketing Status
Marketed Since 2020-12-01
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": "2be8f93f-be67-aef9-e063-6394a90a547e", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["b56dffde-1334-f5a0-e053-2a95a90a717c"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-127-14)", "package_ndc": "72189-127-14", "marketing_start_date": "20201201"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-127-20)", "package_ndc": "72189-127-20", "marketing_start_date": "20201201"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "72189-127_2be8f93f-be67-aef9-e063-6394a90a547e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72189-127", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062505", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}