Package 70095-050-03

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 70095-050-03
Digits Only 7009505003
Product NDC 70095-050
Product ID 70095-050_5ae65432-04a1-4b6b-8536-2535064fc782
Description

25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01)

Marketing

Marketing Status
Marketed Since 2024-03-15
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": "5ae65432-04a1-4b6b-8536-2535064fc782", "openfda": {"upc": ["0370095050014"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["5ae65432-04a1-4b6b-8536-2535064fc782"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70095-050-03)  / 50 mL in 1 VIAL (70095-050-01)", "package_ndc": "70095-050-03", "marketing_start_date": "20240315"}], "brand_name": "SODIUM BICARBONATE", "product_id": "70095-050_5ae65432-04a1-4b6b-8536-2535064fc782", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "70095-050", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Sun Pharmaceutical Industries 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": "20240315", "listing_expiration_date": "20261231"}