Package 70518-4158-0

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 70518-4158-0
Digits Only 7051841580
Product NDC 70518-4158
Description

1 SYRINGE in 1 CARTON (70518-4158-0) / 50 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2024-08-14
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": "3fb730ba-82fd-149f-e063-6394a90afa94", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["792582"], "spl_set_id": ["96093b76-5d98-4d2b-b851-20207a8864db"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (70518-4158-0)  / 50 mL in 1 SYRINGE", "package_ndc": "70518-4158-0", "marketing_start_date": "20240814"}], "brand_name": "Sodium Bicarbonate", "product_id": "70518-4158_3fb730ba-82fd-149f-e063-6394a90afa94", "dosage_form": "INJECTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "70518-4158", "generic_name": "Sodium Bicarbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA203449", "marketing_category": "ANDA", "marketing_start_date": "20240814", "listing_expiration_date": "20261231"}