Package 68001-408-31

Brand: ertapenem

Generic: ertapenem sodium
NDC Package

Package Facts

Identity

Package NDC 68001-408-31
Digits Only 6800140831
Product NDC 68001-408
Description

10 VIAL in 1 CARTON (68001-408-31) / 20 mL in 1 VIAL (68001-408-29)

Marketing

Marketing Status
Marketed Since 2019-08-29
Brand ertapenem
Generic ertapenem sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "12e7c27b-9d21-bf94-e063-6294a90aedcf", "openfda": {"unii": ["2T90KE67L0"], "rxcui": ["1734683"], "spl_set_id": ["8eccc96f-4b59-49ee-9997-365a24f59a24"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (68001-408-31)  / 20 mL in 1 VIAL (68001-408-29)", "package_ndc": "68001-408-31", "marketing_start_date": "20190829"}], "brand_name": "Ertapenem", "product_id": "68001-408_12e7c27b-9d21-bf94-e063-6294a90aedcf", "dosage_form": "INJECTION", "pharm_class": ["Carbapenems [CS]", "Penem Antibacterial [EPC]"], "product_ndc": "68001-408", "generic_name": "Ertapenem Sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ertapenem", "active_ingredients": [{"name": "ERTAPENEM SODIUM", "strength": "1 g/20mL"}], "application_number": "ANDA207647", "marketing_category": "ANDA", "marketing_start_date": "20190829", "listing_expiration_date": "20261231"}