Package 0143-9338-25

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 0143-9338-25
Digits Only 0143933825
Product NDC 0143-9338
Description

25 VIAL in 1 CARTON (0143-9338-25) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-04-26
Brand succinylcholine chloride
Generic succinylcholine chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "07245c04-4789-4b91-9f5e-ab55726042e6", "openfda": {"unii": ["8L0S1G435E"], "rxcui": ["1594589"], "spl_set_id": ["488e1689-84d4-4f96-ac85-fa0cbc661cb6"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9338-25)  / 10 mL in 1 VIAL", "package_ndc": "0143-9338-25", "marketing_start_date": "20210426"}], "brand_name": "Succinylcholine Chloride", "product_id": "0143-9338_07245c04-4789-4b91-9f5e-ab55726042e6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "0143-9338", "generic_name": "Succinylcholine Chloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE DIHYDRATE", "strength": "20 mg/mL"}], "application_number": "ANDA213229", "marketing_category": "ANDA", "marketing_start_date": "20210426", "listing_expiration_date": "20261231"}