Package 0641-6111-10

Brand: Sufentanil Citrate

Generic: Sufentanil Citrate
NDC Package

Package Facts

Identity

Package NDC 0641-6111-10
Digits Only 0641611110
Product NDC 0641-6111
Description

10 AMPULE in 1 CARTON (0641-6111-10) / 2 mL in 1 AMPULE (0641-6111-01)

Marketing

Marketing Status
Marketed Since 1995-12-15
Brand Sufentanil Citrate
Generic Sufentanil Citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INTRAVENOUS"], "spl_id": "638c3fcf-1395-4d3b-885a-a16af800dc9d", "openfda": {"unii": ["S9ZFX8403R"], "rxcui": ["1809097", "1809102", "1809104"], "spl_set_id": ["52fc28b9-464a-4173-9d0d-000ed0dbf265"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (0641-6111-10)  / 2 mL in 1 AMPULE (0641-6111-01)", "package_ndc": "0641-6111-10", "marketing_start_date": "19951215"}], "brand_name": "Sufentanil Citrate", "product_id": "0641-6111_638c3fcf-1395-4d3b-885a-a16af800dc9d", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6111", "dea_schedule": "CII", "generic_name": "Sufentanil Citrate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sufentanil Citrate", "active_ingredients": [{"name": "SUFENTANIL CITRATE", "strength": ".05 mg/mL"}], "application_number": "ANDA074413", "marketing_category": "ANDA", "marketing_start_date": "19951215", "listing_expiration_date": "20261231"}