Package 72603-209-25

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 72603-209-25
Digits Only 7260320925
Product NDC 72603-209
Product ID 72603-209_f2190c6c-50b8-4283-b715-1eabb7e4ff0f
Description

25 VIAL in 1 CARTON (72603-209-25) / 50 mL in 1 VIAL (72603-209-01)

Marketing

Marketing Status
Discontinued 2026-06-30
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": "f2190c6c-50b8-4283-b715-1eabb7e4ff0f", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["068db1fe-0346-48f1-8d2f-8488d7331106"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72603-209-25)  / 50 mL in 1 VIAL (72603-209-01)", "package_ndc": "72603-209-25", "marketing_end_date": "20260630", "marketing_start_date": "20240219"}], "brand_name": "Sodium Bicarbonate", "product_id": "72603-209_f2190c6c-50b8-4283-b715-1eabb7e4ff0f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "72603-209", "generic_name": "SODIUM BICARBONATE", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA216364", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20240219"}