Package 0641-6196-10

Brand: propofol

Generic: propofol
NDC Package

Package Facts

Identity

Package NDC 0641-6196-10
Digits Only 0641619610
Product NDC 0641-6196
Description

10 VIAL, SINGLE-USE in 1 CARTON (0641-6196-10) / 100 mL in 1 VIAL, SINGLE-USE (0641-6196-01)

Marketing

Marketing Status
Marketed Since 2020-05-01
Brand propofol
Generic propofol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "113ac304-ef02-4891-ac8b-8788f4ea041c", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808217", "1808222", "1808224"], "spl_set_id": ["fdb77e13-f5a7-4c4a-9f8e-338b702239c8"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0641-6196-10)  / 100 mL in 1 VIAL, SINGLE-USE (0641-6196-01)", "package_ndc": "0641-6196-10", "marketing_start_date": "20200501"}], "brand_name": "PROPOFOL", "product_id": "0641-6196_113ac304-ef02-4891-ac8b-8788f4ea041c", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0641-6196", "generic_name": "PROPOFOL", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPOFOL", "active_ingredients": [{"name": "PROPOFOL", "strength": "10 mg/mL"}], "application_number": "ANDA074848", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}