Package 68462-951-65

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 68462-951-65
Digits Only 6846295165
Product NDC 68462-951
Product ID 68462-951_f38d0dfc-9bcc-4224-a202-885c9ad0beae
Description

25 VIAL in 1 CARTON (68462-951-65) / 50 mL in 1 VIAL (68462-951-50)

Marketing

Marketing Status
Marketed Since 2025-08-07
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": "f38d0dfc-9bcc-4224-a202-885c9ad0beae", "openfda": {"upc": ["0368462951507", "0368462951651"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["f38d0dfc-9bcc-4224-a202-885c9ad0beae"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (68462-951-65)  / 50 mL in 1 VIAL (68462-951-50)", "package_ndc": "68462-951-65", "marketing_start_date": "20250807"}], "brand_name": "SODIUM BICARBONATE", "product_id": "68462-951_f38d0dfc-9bcc-4224-a202-885c9ad0beae", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "68462-951", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA219701", "marketing_category": "ANDA", "marketing_start_date": "20250807", "listing_expiration_date": "20261231"}