Package 81665-200-25
Brand: sodium bicarbonate
Generic: sodium bicarbonatePackage Facts
Identity
Package NDC
81665-200-25
Digits Only
8166520025
Product NDC
81665-200
Description
25 VIAL in 1 CARTON (81665-200-25) / 50 mL in 1 VIAL (81665-200-01)
Marketing
Marketing Status
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": "ada1be4a-11f4-4850-b98c-88e6ef02cd31", "openfda": {"upc": ["0381665200012"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["aea54f8d-1cdd-4a5c-a2f7-7317ae4c8fbc"], "manufacturer_name": ["OMNIVIUM PHARMACEUTICALS LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 CARTON (81665-200-05) / 50 mL in 1 VIAL (81665-200-01)", "package_ndc": "81665-200-05", "marketing_start_date": "20230616"}, {"sample": false, "description": "25 VIAL in 1 CARTON (81665-200-25) / 50 mL in 1 VIAL (81665-200-01)", "package_ndc": "81665-200-25", "marketing_start_date": "20230616"}], "brand_name": "Sodium Bicarbonate", "product_id": "81665-200_ada1be4a-11f4-4850-b98c-88e6ef02cd31", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "81665-200", "generic_name": "SODIUM BICARBONATE", "labeler_name": "OMNIVIUM PHARMACEUTICALS 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_start_date": "20230616", "listing_expiration_date": "20261231"}