Package 72143-211-60

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 72143-211-60
Digits Only 7214321160
Product NDC 72143-211
Description

60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60)

Marketing

Marketing Status
Discontinued 2026-05-31
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": "74b2de40-77cd-4a58-b648-fbf036f48af0", "openfda": {"upc": ["0372143211606"], "unii": ["19XTS3T51U"], "rxcui": ["1652674"], "spl_set_id": ["37a8cb92-0ade-4fbc-80f7-2ef283bc32cb"], "manufacturer_name": ["JG Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60)", "package_ndc": "72143-211-60", "marketing_end_date": "20260531", "marketing_start_date": "20180420"}], "brand_name": "Doxycycline Hyclate", "product_id": "72143-211_74b2de40-77cd-4a58-b648-fbf036f48af0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72143-211", "generic_name": "Doxycycline Hyclate", "labeler_name": "JG Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20180420"}