Package 72143-262-60

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 72143-262-60
Digits Only 7214326260
Product NDC 72143-262
Product ID 72143-262_10b8bf71-4311-41e8-a891-bab8bc86863f
Description

60 TABLET, FILM COATED in 1 BOTTLE (72143-262-60)

Marketing

Marketing Status
Marketed Since 2025-08-01
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10b8bf71-4311-41e8-a891-bab8bc86863f", "openfda": {"upc": ["0372143262608"], "unii": ["19XTS3T51U"], "rxcui": ["1652674"], "spl_set_id": ["10b8bf71-4311-41e8-a891-bab8bc86863f"], "manufacturer_name": ["JG Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72143-262-60)", "package_ndc": "72143-262-60", "marketing_start_date": "20250801"}], "brand_name": "Doxycycline Hyclate", "product_id": "72143-262_10b8bf71-4311-41e8-a891-bab8bc86863f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72143-262", "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_start_date": "20250801", "listing_expiration_date": "20261231"}