Package 80830-2305-2

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 80830-2305-2
Digits Only 8083023052
Product NDC 80830-2305
Product ID 80830-2305_31343ea0-9185-401b-83f2-f2ae7228bfe4
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (80830-2305-2) / 50 mL in 1 VIAL, SINGLE-DOSE (80830-2305-1)

Marketing

Marketing Status
Marketed Since 2026-01-13
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": "31343ea0-9185-401b-83f2-f2ae7228bfe4", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["ba92f45a-0187-4709-aa70-462b8dae09e9"], "manufacturer_name": ["Amneal Pharmaceuticals Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (80830-2305-2)  / 50 mL in 1 VIAL, SINGLE-DOSE (80830-2305-1)", "package_ndc": "80830-2305-2", "marketing_start_date": "20260113"}], "brand_name": "SODIUM BICARBONATE", "product_id": "80830-2305_31343ea0-9185-401b-83f2-f2ae7228bfe4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "80830-2305", "generic_name": "sodium bicarbonate", "labeler_name": "Amneal Pharmaceuticals Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA217523", "marketing_category": "ANDA", "marketing_start_date": "20260113", "listing_expiration_date": "20271231"}