Package 42023-244-10

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 42023-244-10
Digits Only 4202324410
Product NDC 42023-244
Product ID 42023-244_d3631394-b84d-4dc2-b870-e7c3aa2573b4
Description

10 VIAL in 1 CARTON (42023-244-10) / 10 mL in 1 VIAL (42023-244-01)

Marketing

Marketing Status
Marketed Since 2024-11-26
Brand doxycycline
Generic doxycycline
Sample Package No

Linked Drug Pages (1)

DOXYCYCLINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d3631394-b84d-4dc2-b870-e7c3aa2573b4", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["acb84610-5e26-4b0c-89e5-42bc0f8fa00d"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (42023-244-10)  / 10 mL in 1 VIAL (42023-244-01)", "package_ndc": "42023-244-10", "marketing_start_date": "20241126"}], "brand_name": "DOXYCYCLINE", "product_id": "42023-244_d3631394-b84d-4dc2-b870-e7c3aa2573b4", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "42023-244", "generic_name": "Doxycycline", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA216690", "marketing_category": "ANDA", "marketing_start_date": "20241126", "listing_expiration_date": "20261231"}