Package 83854-001-25

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 83854-001-25
Digits Only 8385400125
Product NDC 83854-001
Description

25 VIAL in 1 CARTON (83854-001-25) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-06-26
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": "38887da2-9f53-8db2-e063-6294a90a7738", "openfda": {"upc": ["0383854001011"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["0df8cf62-4b49-4ec4-aae4-c4a3e6d76549"], "manufacturer_name": ["Anthea Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 CARTON (83854-001-20)  / 50 mL in 1 VIAL", "package_ndc": "83854-001-20", "marketing_start_date": "20250626"}, {"sample": false, "description": "25 VIAL in 1 CARTON (83854-001-25)  / 50 mL in 1 VIAL", "package_ndc": "83854-001-25", "marketing_start_date": "20250626"}], "brand_name": "SODIUM BICARBONATE", "product_id": "83854-001_38887da2-9f53-8db2-e063-6294a90a7738", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "83854-001", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Anthea Pharma Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA219701", "marketing_category": "ANDA", "marketing_start_date": "20250626", "listing_expiration_date": "20261231"}