Package 84549-050-03

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 84549-050-03
Digits Only 8454905003
Product NDC 84549-050
Product ID 84549-050_463cedaa-4d0f-c9b6-e063-6394a90a8b31
Description

50 mL in 1 VIAL (84549-050-03)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

SODIUM BICARBONATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "463cedaa-4d0f-c9b6-e063-6394a90a8b31", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["3867f743-c2cf-a646-e063-6394a90a82e1"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL (84549-050-03)", "package_ndc": "84549-050-03", "marketing_start_date": "20250827"}], "brand_name": "SODIUM BICARBONATE", "product_id": "84549-050_463cedaa-4d0f-c9b6-e063-6394a90a8b31", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "84549-050", "generic_name": "SODIUM BICARBONATE", "labeler_name": "ProPharma Distribution", "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": "20240315", "listing_expiration_date": "20261231"}