Package 67296-2189-2

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 67296-2189-2
Digits Only 6729621892
Product NDC 67296-2189
Description

20 TABLET, FILM COATED in 1 BOTTLE (67296-2189-2)

Marketing

Marketing Status
Marketed Since 2025-03-07
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": "45abfd50-4c78-739f-e063-6394a90a753a", "openfda": {"upc": ["0342806310502"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["44f2fdde-cf84-6f42-e063-6394a90af94e"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (67296-2189-1)", "package_ndc": "67296-2189-1", "marketing_start_date": "20250307"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (67296-2189-2)", "package_ndc": "67296-2189-2", "marketing_start_date": "20250307"}], "brand_name": "Doxycycline Hyclate", "product_id": "67296-2189_45abfd50-4c78-739f-e063-6394a90a753a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "67296-2189", "generic_name": "Doxycycline Hyclate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20250307", "listing_expiration_date": "20261231"}