Package 76329-3352-1

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 76329-3352-1
Digits Only 7632933521
Product NDC 76329-3352
Description

1 SYRINGE in 1 CARTON (76329-3352-1) / 50 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2000-06-01
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": "74a86dc7-0929-40d0-9661-9f9063a8fd7d", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["792582"], "spl_set_id": ["77698221-a01d-4568-a7bc-d3d4e982875d"], "manufacturer_name": ["International Medication Systems, Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (76329-3352-1)  / 50 mL in 1 SYRINGE", "package_ndc": "76329-3352-1", "marketing_start_date": "20000601"}], "brand_name": "Sodium Bicarbonate", "product_id": "76329-3352_74a86dc7-0929-40d0-9661-9f9063a8fd7d", "dosage_form": "INJECTION", "product_ndc": "76329-3352", "generic_name": "Sodium Bicarbonate", "labeler_name": "International Medication Systems, Limited", "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": "20000601", "listing_expiration_date": "20261231"}