Package 24201-201-05

Brand: sodium tetradecyl sulfate

Generic: sodium tetradecyl sulfate
NDC Package

Package Facts

Identity

Package NDC 24201-201-05
Digits Only 2420120105
Product NDC 24201-201
Description

5 VIAL, GLASS in 1 CARTON (24201-201-05) / 2 mL in 1 VIAL, GLASS (24201-201-01)

Marketing

Marketing Status
Marketed Since 2019-12-09
Brand sodium tetradecyl sulfate
Generic sodium tetradecyl sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5c279d1b-193e-46d3-a28c-43a0d3f14f96", "openfda": {"unii": ["Q1SUG5KBD6"], "rxcui": ["204491"], "spl_set_id": ["997394e1-ec1f-4093-e053-2a95a90a0ea0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, GLASS in 1 CARTON (24201-201-05)  / 2 mL in 1 VIAL, GLASS (24201-201-01)", "package_ndc": "24201-201-05", "marketing_start_date": "20191209"}], "brand_name": "Sodium Tetradecyl Sulfate", "product_id": "24201-201_5c279d1b-193e-46d3-a28c-43a0d3f14f96", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "24201-201", "generic_name": "Sodium Tetradecyl Sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Tetradecyl Sulfate", "active_ingredients": [{"name": "SODIUM TETRADECYL SULFATE", "strength": "30 mg/mL"}], "application_number": "ANDA209937", "marketing_category": "ANDA", "marketing_start_date": "20191209", "listing_expiration_date": "20261231"}