Package 82449-000-05

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 82449-000-05
Digits Only 8244900005
Product NDC 82449-000
Description

20 VIAL in 1 CARTON (82449-000-05) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-03-08
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "12d2a9ac-f0d0-e207-e063-6394a90a8f56", "openfda": {"upc": ["0382449000019"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["eb2996b4-c04c-4678-b8a9-5cbbe509bb70"], "manufacturer_name": ["Steriscience Specialties Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 CARTON (82449-000-05)  / 50 mL in 1 VIAL", "package_ndc": "82449-000-05", "marketing_start_date": "20240308"}], "brand_name": "Sodium Bicarbonate", "product_id": "82449-000_12d2a9ac-f0d0-e207-e063-6394a90a8f56", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "82449-000", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Steriscience Specialties Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA217594", "marketing_category": "ANDA", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}